A U.S. grocery store aisle (representative file photo). Specific recalled product: see recall details below. Photo: Tessa Bury / Wikimedia Commons (CC BY 4.0).
Recall Database
Other Injury Hazards Recalls
This is the catch-all hub — 314 records that don't fall cleanly into one of the named hazard classes. The mix is 273 FDA, 34 CPSC, and 7 NHTSA. A record lands here when its recall text describes a hazard the taxonomy's named rules don't capture; it is the deliberate residual — the bucket for recalls whose own wording doesn't match a named hazard, which keeps the named hubs precise.
Because the reason is varied, this hub is best browsed rather than searched by a single hazard. It is worth checking if a product you're looking for isn't in the hazard hub you expected — the classification follows the recall's own wording, which doesn't always match a consumer's mental category.
The notices span 2023–2026, heaviest in 2026. Every row links to the original FDA, CPSC, or NHTSA notice with the recall reason and the remedy.
How this hub is built. This page groups the 314 recall records that 411 Press classifies as Other Injury Hazards. Each record gets one primary hazard from a fixed, published rule set (taxonomy version 2026-07-28.C2.2 — this stamp marks when the classification rules last changed, not how current the recall data is; data currency is stated below). A record can carry secondary hazard tags but appears on only one hub. Regulators in this hub: FDA (273), CPSC (34), NHTSA (7). These notices were published 2023–2026. This is not an all-time archive — it is the current dataset, drawn from CPSC, FDA, and NHTSA notices and refreshed as new notices are ingested from the agency feeds, so it grows over time. A note on counting. This hub counts RECORDS, not recall events. The agencies package recalls differently — NHTSA issues one record per safety campaign, the CPSC one per recall, the FDA one per affected product line — so an FDA-heavy hub carries more product-line records per underlying recall than a CPSC or NHTSA one. Records here are grouped by hazard; the brand hubs, which rank companies, count by event instead. Every row links to the original agency notice. The agency's record is the authority; the hazard grouping is ours. For a small number of records the agency feed's own hazard text did not pass our integrity check; those rows read "See the agency notice for the hazard description" and link straight to the source, rather than show a summary we can't stand behind.
2026 (260)
- FDAClass II
Mycophenolate Mofetil for Injection USP
Presence of precipitate
- FDAClass II
Mellish Island Super Skin; Dietary Supplement; 60 Capsules, 2 per day; Distributed by Mellish Island Corp
Firm's finished product label does not declare the source of marine collagen which was determined to be fish.
- FDAClass I
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.
- FDAClass II
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT
Potential for spoilage.
- FDAClass II
Buprenorphine HCl
Crystallization; identified as Buprenorphine free base
- FDAClass I
ABIOMED Introducer Kit 23 Fr
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Intro Kit
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Insertion Kit, Pkgd, JP, Pump Set Code 0052-0011-JP; containing Introducer Product Code 0052-3006-JP
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella RP Flex with SmartAssist Set
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Smart Assist Set, JP, Pump Set Code 0048-0024-JP; containing Introducer Product Code 0052-3025-JP
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Set, Pump Set Code 0048-0044; containing Introducer Product Code 0052-3046
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Set, Pump Set Code 0048-0014; containing Introducer Product Code 0052-3046
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Set
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Introducer Kit 14 Fr
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Introducer Kit 14 Fr
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella CP Introducer Kit 14 Fr
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella 5.5 SmartAssist S2 Set
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- FDAClass I
ABIOMED Impella 5.5 Smart Assist Set
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- CPSCInfo
Model Year 2019-2025 UMAX Bistro and Bistro Deluxe Vehicles
The recalled Bistro and Bistro Deluxe vehicles have an inaccurate weight capacity certification label. This could result in the vehicle being overloaded, which poses an injury hazard.
- FDAClass II
Plastic 1-gallon clear pail blue label which reads in part as "BLUE RIBBON CLASSICS FRENCH VANILLA, MFD
Elevated coliforms
- FDAClass I
Abiomed REF: 0052-3025
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.
- FDAClass I
Abiomed REF: 0052-3021
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines in the hub region.
- FDAClass II
Gemcitabine Injection
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
- CPSCWarning
Children's Tiny Land Play Tents
The recalled tents' fiberglass poles can shed fibers, posing an injury risk of skin and eye irritation.
- FDAClass II
Total Parental Nutrition - Pediatric PN Patient-Specific TPN Bag
Incorrect product formulation: bag did not contain copper and famotidine per label.
- FDAClass II
Aripiprazole Tablets USP
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
- FDAClass II
functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY COMPLETE PLANT BASED
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- FDAClass II
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- FDAClass I
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13
Potential for thrombus formation during prolonged use of the introducer.
- FDAClass I
Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits
Potential for thrombus formation during prolonged use of the introducer.
- FDAClass I
Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP
Potential for thrombus formation during prolonged use of the introducer.
- FDAClass I
Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP
Potential for thrombus formation during prolonged use of the introducer.
- FDAClass II
Fairhope Roasting Company Cold Brew Coffee Concentrate
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
- CPSCInfo
Orb Funkee Squeeze Toys
The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.
- FDAClass II
Farm Rich Pizza Cheese Crunchers
May contain metal pieces
- FDAClass I
Impella CP Set with SmartAssist
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
- FDAClass II
VistaPharm
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- FDAClass II
VistaPharm
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- FDAClass II
VistaPharm
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- FDAClass II
VistaPharm
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
- FDAClass III
Salt
Plain salt was labeled as iodized and iodized salt was labeled as plain.
- FDAClass II
Lunds & Byerly's Curry Powder Sweet
Sesame Seeds White were labeled as Curry Powder Sweet.
- FDAClass I
Panda Freestanding Warmer
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
- FDAClass I
Giraffe Warmer with Integrated Resuscitation System (iRes)
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
- FDAClass I
Giraffe Stand-alone Infant Resuscitation System
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting in hypoxia or hyperoxia in the patient.
- FDAClass I
Atlan A350XL
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- FDAClass I
Atlan A350
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
- FDAClass II
NEURO NOURISH dietary supplement
Premature lipid oxidation causing quality issue potentially causing product to have an off odor and bitter taste.
- FDAClass I
Medline Convenience Kits: 1) OPEN HEART CDS
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- FDAClass I
Medline Convenience Kits: 1) DYNJ905503F
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- FDAClass I
Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- FDAClass I
Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP which were recalled due to quality issues identified during a recent FDA inspection of the supplier.
- FDAClass I
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
- FDAClass I
Spinal Needle procedure kits: Material Description (Material Number) 24GA
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
- FDAClass I
Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
- FDAClass II
UPC 29787600000 Kitchen SALAD CAESAR LARGE SS COLD UPC 21543200000 Kitchen SALAD CAESAR SMALL SS COLD This is
Contains statement does not declare Anchovy
- FDAClass II
UPC 29787500000 KITCHEN SALAD SPRING LARGE This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass III
UPC 29604300000 SALMON WASABI GRILLED FS COLD This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Salmon
- FDAClass III
UPC 29502200000 Ready Meals BOWL GRAIN SALMON QUINOA LENTIL SS COLD This is Albertson's store-made item and sold
Contains statement does not declare Salmon
- FDAClass II
UPC 29477800000 Ready Meals SALAD SEAFOOD CAJUN SS COLD UPC 29477600000 SALAD SEAFOOD CAJUN FS COLD This is Albertson's
Contains statement does not declare Crab and Pollock
- FDAClass III
UPC 29473400000 SALAD LEMON CAPELLINI With GRILLED SHRIMP FS This is Albertson's store-made item and sold by random
Contains statement does not declare Shrimp
- FDAClass II
UPC 29472300000 SALAD KALE BERRY FETA FS COLD UPC 29472100000 Ready Meals SALAD KALE BERRY FETA SS COLD This is
Contains statement does not declare Walnut
- FDAClass II
UPC 29433900000 Kitchen SALAD CHICKEN STRIP This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass II
UPC 29361000000 KITCHEN SALAD TURKEY POPPYSEED SS COLD UPC 29360900000 KITCHEN SALAD TURKEY POPPYSEED FS COLD This is
Contains statement does not declare Almond
- FDAClass II
UPC 29344500000 TWISTED BLISS PRETZEL TRAY This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass II
UPC 29259700000 KITCHEN TRAY SUB SANDWICH SS This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio
- FDAClass III
UPC 29251100000 Ready Meals TUNA SALAD & PEPPER JACK CHEESE SNACKER This is Albertson's store-made item and sold
Contains statement does not declare Tuna
- FDAClass III
UPC 29219100000 Ready Meals SANDWICH HAGGIE STORE CLASSIC TUNA SS COLD This is Albertson's store-made item and sold
Contains statement does not declare Tuna
- FDAClass II
UPC 29168800000 CARVING TRAY 16IN FS This is Albertson's store-made item and sold by unit at point of sale with grocery
Contains statement does not declare Walnut
- FDAClass II
UPC 29153000000 SAMPLER TRAY ITALIAN 16 INCH This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass II
UPC 29138800000 TRAY CHARCUTERIE ELEGANT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio
- FDAClass II
UPC 29133000000 TRAY COCKTAIL This is Albertson's store-made item and sold by unit at point of sale with grocery
Contains statement does not declare Almond
- FDAClass III
UPC 29132100000 KITCHEN SNACKER SALAD TUNA PICKLE This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Tuna
- FDAClass III
UPC 29120700000 Ready Meals SALAD SMOKED SALMON & FETA PASTA SS UPC 29137800000 SALAD SMOKED SALMON & FETA PASTA FS
Contains statement does not declare Salmon
- FDAClass II
UPC 28994500000 PAVILIONS MUFFINS BANANA NUT SINGLE SERVE This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Walnut
- FDAClass III
UPC 28848900000 Cake Yellow Fudge Pecan 1/2 8IN This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare pecan.
- FDAClass III
UPC 28832500000 Cake Yellow Caramel Pecan 1/2 8IN UPC 28831600000 Cake Yellow Caramel Pecan 2-Layer These are
Contains statement does not declare pecan.
- FDAClass III
UPC 28586600000 CROISSANT ALMOND UPC 22102100000 CROISSANTS ALMOND 4 CT UPC 29671400000 HGN CROISSANTS ALMOND 3CT This
Contains statement does not declare Almond
- FDAClass III
UPC 27852000000 Ready Meals BRIE ALMOND TRAY SMALL COLD This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond
- FDAClass II
UPC 27841000000 Ready Meals TRAY BRIE & BLEU CHEESE LARGE This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond
- FDAClass II
UPC 27837800000 PLATTER CHEESES OF FRANCE This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass II
UPC 27183100000 Ready Meals DUO SEAFOOD SALAD W/CRACKERS This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Whiting
- FDAClass II
UPC 27163100000 Kitchen SALAD GRILLED CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond
- FDAClass II
UPC 26911700000 COOKIES OATMEAL RAISIN 10CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass II
UPC 25814700000 CAKE BOSTON CREME DUBAI 5IN This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio.
- FDAClass II
UPC 25811100000 CAKE RASPBERRY MOON 8IN 2-layer
Contains statement does not declare Almond.
- FDAClass III
UPC 25800800000 POP DOTS COCO & HAZELNUT 6CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare hazelnut
- FDAClass III
UPC 25748400000 STICKY BUNS GOURMET WALNUT 4CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Walnut
- FDAClass II
UPC 25688000000 PIE PEACH MELBA 9IN This is Albertson's store-made item and sold by unit at point of sale with grocery
Contains statement does not declare Almond
- FDAClass II
UPC 25678000000 CROISSANTS DUBAI CHOCOLATE 2CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio
- FDAClass II
UPC 25606600000 PARFAIT CUP DUBAI CHOCOLATE This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio
- FDAClass II
UPC 25524000000 MUFFINS STICKY BRAN 4CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Walnut
- FDAClass II
UPC 25511500000 PLATTER BROWNIES ASSORTED SEASONAL This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Walnut
- FDAClass II
UPC 25491700000 Cake Pav Chocolate Lady Madeleines Strawberry
Contains statement does not declare Almond.
- FDAClass III
UPC 25394400000 CAKE PISTACHIO SHAPED DESSERT 1CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio.
- FDAClass III
UPC 25317100000 CROISSANTS ALMOND RASPBERRY FILLED 4CT This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond
- FDAClass II
UPC 25312600000 MUFFINS BANANA NUT CREAM CHEESE FILLED 2CT This is Albertson's store-made item and sold by unit
Contains statement does not declare Walnut
- FDAClass II
UPC 25216200000 Cheesecake Slice Colossal Dubai
Contains statement does not declare pistachio.
- FDAClass II
UPC 25185700000 COOKIE GOURMET DUBAI 1CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pistachio.
- FDAClass II
UPC 25139500000 Cake Cakerie Strawberry Shortcake Triangle
Contains statement does not declare Hazelnut.
- FDAClass II
UPC 25081900000 PLATTER PASTRY MINI BREAKFAST 28CT This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond
- FDAClass II
UPC 25047100000 ANDRONICO'S SWEET START CATERING TRAY LARGE This is Albertson's store-made item and sold by unit
Contains statement does not declare Walnut
- FDAClass II
UPC 24512800000 SALAD CHICKEN CAESAR UPC 29854600000 Kitchen SALAD CHICKEN CAESAR This is Albertson's store-made item
Contains statement does not declare Anchovy
- FDAClass II
UPC 24144500000 Ready Meals PEANUT BUTTER CHOCOLATE CHIP BAR With PRETZEL This is Albertson's store-made item and sold
Contains statement does not declare Almond
- FDAClass II
UPC 23952700000 POKE AHI LIMU UPC 23506700000 POKE AHI LIMU PREVIOUSLY FROZEN - CO UPC 23958200000 POKE AHI SALT &
Contains statement does not declare Tuna
- FDAClass II
UPC 23625000000 FISH HOUSE PREMIUM SEAFOOD SALAD UPC 21431200000 Ready Meals SALAD SEAFOOD SS UPC 21878600000 SALAD
Contains statement does not declare Crab
- FDAClass III
UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson's store-made item and sold by random weight at point of sale
Contains statement does not declare Tilapia
- FDAClass II
UPC 23285600000 IMITATION CRAB AND SHRIMP SALAD SRIRACHA This is Albertson's store-made item and sold by random weight
Contains statement does not declare Pollock
- FDAClass II
UPC 23285300000 IMITATION CRAB AND SHRIMP SALAD This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Pollock
- FDAClass III
UPC 23258300000 BURGER WILD SALMON FETA SPINACH This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Salmon
- FDAClass II
UPC 23245700000 SHRIMP & SURIMI CEVICHE FRESH This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Sea Bream
- FDAClass III
UPC 23180600000 SALMON KABOB With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 23180100000 SHRIMP KABOB 16-20 CT W/KUNG PAO MRND This is Albertson's store-made item and sold by random weight
Contains statement does not declare Shrimp.
- FDAClass III
UPC 23179700000 SHRIMP KABOB 16-20 CT With JAMAICAN JRK MARINADE This is Albertson's store-made item and sold by random
Contains statement does not declare Shrimp.
- FDAClass II
UPC 23168600000 SHRIMP 41-50 P&D With CILANTRO LIME MARINADE 5% This is Albertson's store-made item and sold by random
Contains statement does not declare Shrimp and Anchovy
- FDAClass III
UPC 23152800000 SHRIMP 41-50 P&D With JAMAICAN JERK MARINADE 5% This is Albertson's store-made item and sold by random
Contains statement does not declare Shrimp.
- FDAClass III
UPC 23151700000 SALMON FILLET With CITRUS LEMON MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 23150400000 SHRIMP 41-50 P&D With CITRUS LEMON MARINADE 5% This is Albertson's store-made item and sold by random
Contains statement does not declare Shrimp.
- FDAClass II
UPC 23114800000 SEAFOOD SALAD IMITATION CAJUN CRAB This is Albertson's store-made item and sold by random weight
Contains statement does not declare Crab and Pollock
- FDAClass III
UPC 23100200000 SALMON ATLANTIC PORTION PIRI PIRI MARINADE This is Albertson's store-made item and sold by unit
Contains statement does not declare Salmon
- FDAClass III
UPC 23098000000 SALMON ATLANTIC PORTION CA ORANGE MARINADE This is Albertson's store-made item and sold by unit
Contains statement does not declare Salmon
- FDAClass III
UPC 23090400000 SALMON FILLET POLLO ASADO MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 23077600000 SALMON FILLET CARNE ASADA MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 23070400000 SHRIMP SKEWER MEDIUM RAW CILANTRO LIME This is Albertson's store-made item and sold by random weight
Contains statement does not declare Shrimp.
- FDAClass III
UPC 23044100000 SHRIMP P&D CAJUN SEASONED This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Shrimp.
- FDAClass III
UPC 23043800000 SHRIMP 16-20 KABOB POLLO ASADA MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Shrimp
- FDAClass III
UPC 23041600000 SALMON COHO FILLET GARLIC HERB SEASONED This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 23036500000 SHRIMP P&D OLD BAY SEASONED This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Shrimp.
- FDAClass III
UPC 23025600000 SHRIMP MEDIUM SWEET CHILI MARINADE This is Albertson's store-made item and sold by random weight
Contains statement does not declare Shrimp.
- FDAClass III
UPC 22761900000 MUFFINS ALMOND POPPYSEED 4CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Almond
- FDAClass III
UPC 22749800000 CAKE BOSTON ALMOND This is Albertson's store-made item and sold by unit at point of sale with grocery
Contains statement does not declare Almond.
- FDAClass II
UPC 22730900000 COOKIES COWBOY 18CT This is Albertson's store-made item and sold by unit at point of sale with grocery
Contains statement does not declare Pecan
- FDAClass II
UPC 22679400000 CAKE CRAVIN CARROT 8IN 1-layer This is Albertson's store-made item and is sold by each unit at point
Contains statement does not declare pecan.
- FDAClass II
UPC 22655200000 CAKE CARROT 8IN 2-Layer UPC 27813200000 CAKE CARROT 8IN 2-Layer These are Albertson's store-made items
Contains statement does not declare pecan or walnut.
- FDAClass II
UPC 22650200000 PLATTER LOAF SLC 20CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Walnut
- FDAClass II
UPC 22454900000 MUFFINS BANANA NUT 2CT UPC 22120200000 MUFFINS BANANA NUT 4CT This is Albertson's store-made item
Contains statement does not declare Walnut
- FDAClass II
UPC 22418000000 Platter Catering Loaf Cake Slice
Contains statement does not declare Walnut.
- FDAClass III
UPC 22394700000 Cake Almond Raspberry Pavillions 2-layer This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Almond.
- FDAClass II
UPC 22358600000 COOKIES MEXICAN WEDDING 8 CT This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Pecan
- FDAClass II
UPC 22321200000 MUFFINS PISTACHIO 2CT UPC 22770600000 MUFFINS PISTACHIO 4CT This is Albertson's store-made item
Contains statement does not declare Walnut
- FDAClass II
UPC 22304700000 PLATTER SNACK CHEWIE SUSANS THUMBPRINTS This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Pecan
- FDAClass II
UPC 22253500000 Cake Bar Artisan White Strawberry Small
Contains statement does not declare Almond.
- FDAClass II
UPC 22019700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 1 CT UPC 22117700000 PAVILIONS CHOCOLATE COVERED STRAWBERRY 4 CT
Contains statement does not declare Hazelnut
- FDAClass III
UPC 21963800000 Ready Meals CHIMICHURRI SHRIMP BOWL SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Shrimp
- FDAClass III
UPC 21919300000 SALMON LEMON PEPPER KOSHER PO SS COLD This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass III
UPC 21914600000 KITCHEN SANDWICH CROISSANT CHICKEN CASHEW SS This is Albertson's store-made item and sold by unit
Contains statement does not declare Cashew
- FDAClass III
UPC 21877300000 SALMON SWEET CHILI KOSHER PO SS COLD This is Albertson's store-made item and sold by random weight
Contains statement does not declare Salmon
- FDAClass II
UPC 21870200000 KITCHEN SALAD SESAME ASIAN LARGE SS COLD UPC 27817500000 Ready Meals SALAD MANDARIN SESAME NOODLE SS
Contains statement does not declare Almond
- FDAClass III
UPC 21843300000 READY MEALS TUNA SALAD & MUENSTER CHEESE SNACK PACK This is Albertson's store-made item and sold
Contains statement does not declare Tuna
- FDAClass III
UPC 21788400000 Ready Meals SANDWICH TUNA SALAD CROISSANT SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare TUNA
- FDAClass II
UPC 21633500000 READY MEALS SALAD APPLE WALDORF SS UPC 29824500000 Kitchen SALAD APPLE WALDORF FS UPC 27169500000
Contains statement does not declare Walnut
- FDAClass II
UPC 21600500000 READY MEALS SALAD PREMIUM BROCCOLI SS This is Albertson's store-made item and sold by random weight
Contains statement does not declare Cashew
- FDAClass III
UPC 21535300000 TEMPURA SHRIMP THAI SWEET CHILI SAUCE SS This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Shrimp.
- FDAClass III
UPC 21500300000 READY MEALS QUAD TUNA SALAD This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Tuna
- FDAClass III
UPC 21497700000 Ready Meals SALMON POT ROSETTES & ROSEMARY SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Salmon
- FDAClass III
UPC 21495100000 Ready Meals MEAL SALMON CAJUN SS COLD This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Salmon
- FDAClass III
UPC 21494500000 Ready Meals MEAL SALMON With LEMON CAPELLINI PASTA SS This is Albertson's store-made item and sold
Contains statement does not declare Salmon
- FDAClass II
UPC 21478000000 Ready Meals SALAD FRESH BERRY & SWEET CHILI Salmon SS This is Albertson's store-made item and sold
Contains statement does not declare Salmon and Walnut
- FDAClass II
UPC 21477700000 Ready Meals SALAD FRESH BERRY & SALMON SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Salmon and Walnut
- FDAClass III
UPC 21467900000 Ready Meals BOWL SOUTHWEST SHRIMP LARGE SS COLD UPC 21963600000 Ready Meals SOUTHWEST SHRIMP BOWL SS
Contains statement does not declare Shrimp
- FDAClass II
UPC 21425300000 READY MEALS SALAD KALE MANGO & COCONUT SS UPC 21042400000 SALAD KALE MANGO & COCONUT FS This is
Contains statement does not declare Cashew
- FDAClass II
UPC 21409600000 READY MEALS MEATLOAF SS COLD This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Anchovy
- FDAClass III
UPC 21382900000 Ready Meals SALMON PESTO With ASPARAGUS SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Salmon
- FDAClass II
UPC 21380100000 Ready Meals WOK PAD THAI CHICKEN WITH POT STICKERS SS This is Albertson's store-made item and sold
Contains statement does not declare Anchovy
- FDAClass II
UPC 21379600000 Ready Meals WOK PAD THAI CHICKEN WITH EGG ROLL SS COLD This is Albertson's store-made item and sold
Contains statement does not declare Anchovy
- FDAClass III
UPC 21330300000 Ready Meals BAKED POLLOCK 4CT SS COLD This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Pollock
- FDAClass II
UPC 21299900000 LOX AVOCADO TOAST FS COLD This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Salmon
- FDAClass III
UPC 21292200000 SALMON CAJUN PREMIUM FS COLD This is Albertson's store-made item and sold by unit at point of sale
Contains statement does not declare Salmon
- FDAClass II
UPC 21243500000 KITCHEN SANDWICH ITALIAN SUPER SUB SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Pistachio
- FDAClass III
UPC 21234900000 TILAPIA PARMESAN CRUSTED SS COLD This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Tilapia
- FDAClass II
UPC 21208300000 Ready Meals WOK PAD THAI CHICKEN SS COLD This is Albertson's store-made item and sold by random weight
Contains statement does not declare Anchovy
- FDAClass II
UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store-made item and sold by unit
Contains statement does not declare Walnut
- FDAClass II
UPC 21176300000 MEAT PIE PORK 4CT SS COLD UPC 21025900000 PIE PORK FS COLD This is Albertson's store-made item and sold
Contains statement does not declare Anchovy
- FDAClass II
UPC 21163600000 Ready Meals SALAD WALDORF SS This is Albertson's store-made item and sold by random weight at point
Contains statement does not declare Walnut
- FDAClass III
UPC 21142400000 MEAL CAJUN SALMON & SPANISH RICE SS COLD This is Albertson's store-made item and sold by unit at point
Contains statement does not declare Salmon
- FDAClass III
UPC 21136500000 Ready Meals BOWL SALMON TERIYAKI SS COLD UPC 21477800000 Ready Meals BOWL TERIYAKI SALMON LARGE SS COLD
Contains statement does not declare Salmon
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass I
Medline kits containing Huons Co
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
- FDAClass II
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be
Due to nonconforming products being inadvertently distributed.
- FDAClass II
SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
- FDAClass II
3DIMENSIONS MAMMOGRAPHY SYSTEM
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
- FDAClass II
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp
Product has the potential for false positive results
- FDAClass II
Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
- FDAClass II
Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485
Respiratory/sore throat panel test may result in false negative results and control failures.
- FDAClass II
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
- NHTSAWarning
2023–2025 Toyota Corolla Cross Hybrid
Insufficient pedestrian warning sounds may fail to alert pedestrians of a reversing vehicle, increasing the risk of injury.
- FDAClass II
Philips Azurion
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to the forces applied when the monitor is moved or rotated.
- FDAClass II
Straumann n!ce Zr, HT, Full-arch Restoration
Includes an incorrect screw seat interface.
- FDAClass II
Straumann n!ce PMMA Full-arch Restoration
Includes an incorrect screw seat interface.
- FDAClass II
Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon bucket/pail - white round food and freezer grade
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- FDAClass II
Zarlengo's Chocolate Gelato packaged in multiple sizes
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- FDAClass II
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
- FDAClass II
Immy
Neutralization Buffer may contain contaminants
- FDAClass II
Pantoprazole Sodium
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
- FDAClass II
Yeastone Broth, 11ML, 10/BOX YY3462
Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
- FDAClass II
Protocol Configuration Tool (PCT) software v1.3.0 for Hamilton AutoLys STAR used within FoundationOneCDx (F1CDx)
Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys Hamilton STAR.
- FDAClass II
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110
The non-tamperproof battery door supplied with the sound processor fails to conform to IEC 60601-1-11:2015 by not requiring the use of a tool to replace the button/coin cell battery.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
QC Quality Choice
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
MGC Health
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
MGC Health
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
MGC Health
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
exchange select
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
exchange select
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
caring mill
This recall is being initiated following FDA's recommendation based on certain observations noted during an August 15, 2025, inspection of the manufacturing facility that may bear on product quality.
- FDAClass II
Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx)
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variants
- FDAClass III
Raw & Unfiltered Bee Well Wildflower Honey NET wT
High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content.
- FDAClass II
Riverence Smoked Trout Dip, net wt
Label declares cream cheese but does not declare milk
- FDAClass II
Philips AneurysmFlow
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable prognostic information regarding aneurysm occlusion following Flow Diverter Stent treatment, however despite being stated in the IUF, it is being relied on for making clinical decisions.
- FDAClass II
Brand Name: Leksell Vantage Arc System REF: 1053958
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
- FDAClass I
Magnesium Sulfate in Water for Injection
Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.
- FDAClass II
Albuterol Sulfate Inhalation Solution
Labelling: Illegible label
- FDAClass II
Buprenorphine Hydrochloride
Crystallization; identified as Buprenorphine free base
- FDAClass III
Yunker(branded) Energy & Health Herbal Supplement with Vitamins; Manufactured by Sato Pharmaceuticals Co
Product does not meet label claim for Vitamin E.
- FDAClass II
LinkBio CORE Workstation, a component of the CORE Shoulder System
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
- FDAClass II
Favorina Chocolate Ladybugs German-Style Nougat, Net Wt 3.52 oz (100g)
Label does not specify type of tree nut contained in the product.
- FDAClass I
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
- FDAClass II
Horizon Organic Chocolate Organic Lowfat Milk
Package integrity compromised.
- FDAClass II
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the load, leading to rapid and uncontrolled downward movement of the lifting arm.
- FDAClass II
nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
- FDAClass II
The product is a handheld ultraviolet-C germicidal wand and contains a combination of five UV-A and UV-C LED lights
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
- FDAClass II
The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure mercury bulbs with a peak
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety guidelines for skin and eye exposure.
- FDAClass II
CUSA Clarity C7000 Console, Software Version: 2.1.1.909
Software issue that renders the touch screen unresponsive.
- FDAClass II
Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
- FDAClass III
WeiKFiELD Custard Powder Kesar Pista, Net Wt
The ingredient, Pista, currently declared on our label should be corrected to the standard American nomenclature, Pistachio.
- FDAClass II
Imu-Tek Colostrum-5 Powder
Product is potentially under-processed.
- FDAClass II
Imu-Tek Colostrum-5 120 Capsules
Product is potentially under-processed.
- FDAClass II
Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE
Due to a quality issue regarding the presence of burr on the finished cervical plate product.
- FDAClass I
Prime Food Processing Dried Croaker Fish
Uneviscerated Fish
- FDAClass II
Coco's Italian Market Heat-n-Eat Fettuccini Alfredo in homemade Alfredo Sauce, Net Wt
Label lists semolina and durum flour as sub-ingredients of the pasta, but does not declare wheat
- FDAClass II
Coco's Italian Market Cannoli Making Kit with 6 Cannoli Shells & Cream, Net Wt
Label lists flour as a sub-ingredient of the shells, and ricotta cheese as a sub-ingredient of the cream but does not declare wheat or milk.
- FDAClass II
Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel
Ingredients List declares peanut but the Contains statement does not declare peanut
- CPSCInfo
Urban Arrow FamilyNext Pro Cargo E-Bikes
The buckle can fail to fully latch when used with children in the cargo area, posing injury hazards to children.
- FDAClass III
Doxazosin Tablets
Tablets/Capsules Imprinted with Wrong ID
- FDAClass I
UDENYCA
Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.
- FDAClass III
Mung Beans packaged in 4lb polybags; 6-4lb bags per carton
Presence of Thiamethoxam-PESTICIDE
- FDAClass II
Isotretinoin Capsules
Superpotent and Subpotent
- FDAClass II
Isotretinoin Capsules
Superpotent and Subpotent
- FDAClass I
Modern Warrior Ready, Dietary Supplement, 60 CAPSULES
FDA analysis revealed the presence of unapproved ingredients including tianeptine, 1,4 DMAA, and aniracetam.
- FDAClass II
Mint Lesion; Software Versions: 3.4.0 up to 3.9.5
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly linked to other patients.
2025 (26)
- FDAClass II
Levothyroxine Sodium Tablets
Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets.
- FDAClass II
CHIPS AHOY
Hard corn starch lumps were found in the product
- FDAClass I
WHILL Model F
Cyber vulnerability of BLE communication was found by CISA VDP program.
- FDAClass I
WHILL Model C2
Cyber vulnerability of BLE communication was found by CISA VDP program.
- FDAClass II
TPN bag (patient specific)
Incorrect Product Formulation: product did not contain insulin as listed in the label.
- FDAClass III
Willy Pete's Chocolates brand Almond Despair
Almonds are not declared in the ingredient statement. Almond is included in description of product on front label.
- FDAClass II
BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v)
Lack of Assurance of Sterlity
- FDAClass II
Sapori Amaretti Almonds 175 g Cookies
Contains elevated levels of hydrocyanic acid
- FDAClass II
McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt
Product is labeled as decaf, but might contain caffeine.
- CPSCWarning
Primark Water Balloon Pump
The water balloon pump can generate excessive pressure during use, causing the product to rupture, posing a risk of physical injury to the user or bystanders.
- FDAClass III
Lost and Found Energy
Recall is due to a misprint on the label that incorrectly identifies the total caffeine content on the can. The item contains 300mg of caffeine, instead of 150mg as provided on the can.
- FDAClass III
Morphine Sulfate Oral Solution 100 mg / 5 mL (20 mg* / mL)
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
- FDAClass II
Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution
Incorrect Product Formulation
- CPSCInfo
Destination Holiday Glow Light Stick Bracelets
The green glow stick bracelet within the 12-pack container can leak, posing a skin irritation hazard.
- FDAClass I
SiluetaYa Mexican Tejocote Roots Supplement Pieces
Product contains yellow oleander
- FDAClass III
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2
Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.
- FDAClass III
OptiWize Health OptiWize Collagen Plus 320 count bottle; White bottle with black lid
The firm initiated a voluntary recall after NSF testing showed that labeled ingredient quantities did not align with analytical test results, manganese level was below label quantity.
- FDAClass I
Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
- CPSCWarning
Vevor Single Post Handrails
The handrails' welding can break while a consumer is holding onto the handrail when stepping down a flight of stairs, posing an injury hazard.
- CPSCWarning
Holiday Lane Infant Footed Pajamas
The elastic on the pajamas' ankles can be too tight and restrict blood circulation, posing an injury hazard.
- FDAClass II
Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during the prime cycle or treatment phase, leading to a delay in patient treatment and blood loss.
- NHTSAWarning
2024 Ford Bronco
A malfunctioning child safety lock that allows a rear door to be opened unintentionally can increase the risk of injury.
- CPSCInfo
Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
The fasteners on the vehicle's rollover protective structure (ROPS) pillar joints can be missing or loose and fail to protect the occupants, if the vehicle rolls over or tips over. This poses an injury hazard.
- FDAClass II
Frosted Almond; 20 lbs (bulk); No UPC# Bulk Product Code: 23208
elevated levels of aflatoxin
- CPSCCritical
BD Recon LT Avalanche Transceivers
The metal contact in the switch mechanism of the Recon LT avalanche transceiver can corrode and cause the transceiver to malfunction. If this occurs, the device can turn off and make it impossible to locate a victim in an avalanche, which could result in serious injury or death.
- NHTSAWarning
2022–2024 BMW X3
Doors that can be inadvertently unlocked and unlatched may open unexpectedly, increasing the risk of injury to rear seat occupants.
2024 (17)
- CPSCCritical
PIEPS Pro IPS Avalanche Transceivers
The battery compartment within the avalanche transceiver could not have enough contact force to supply power. In some cases, the transceiver will fail to power on or cease operating during use. It would make it impossible to locate a victim in an avalanche emergency situation, which could result in serious injury or death.
- NHTSAWarning
2024–2025 Kia Ev9
Seats without mounting bolts may not properly restrain an occupant, increasing the risk of injury.
- CPSCWarning
Cultivar Planter Boxes
The recalled planter box frame can break, posing an injury hazard.
- CPSCWarning
Ceiling Hoists with Straps
The plastic buckles on the straps being used to hold a kayak, canoe or other large objects with the ceiling hoist can break, posing an injury hazard to consumers.
- NHTSAWarning
2021–2024 Volkswagen Id.4
A vehicle door that opens unexpectedly while driving increases the risk of injury.
- CPSCWarning
Squeeze Plush Ball Toys
The squeeze ball toy contains a liquid and glitter combination inside a thick membrane. If the membrane is ruptured, the glittery water can splash onto a child's face and body, posing an injury hazard.
- CPSCWarning
Berkley Jensen Gazebos
The gazebo's roof panels can dislodge in high winds, posing an injury hazard.
- CPSCWarning
Finger-Ease Guitar String Lubricants
The recalled guitar string lubricant contains a contaminant, posing a risk of skin irritation.
- CPSCInfo
Daikin FIT, Amana Brand S-series, and Goodman SD heat pumps
A power interruption in the heat pump can result in the product providing heat when the power resumes, despite the thermostat being in cooling mode, posing a risk of excessive heat exposure to consumers.
- CPSCInfo
Wild Country Ropeman 1 ascenders
The teeth of the recalled ascenders can fail to engage, making it difficult or impossible for the user to ascend.
- CPSCInfo
Oregon, PowerPro, Country Tuff, and Speeco branded log splitters and cylinder kits
The recalled log splitter's hydraulic cylinder rod can separate from the piston, preventing the wedge from retracting. Reengaging the rod to the piston can cause the rod and wedge to move unexpectedly, posing injury hazards.
- CPSCInfo
Crosman Icon Air Rifles
An uncocked and loaded air rifle can discharge unexpectedly if jolted or dropped, posing an injury hazard.
- CPSCInfo
3M™ Peltor™ X4 Series Earmuffs
The recalled noise-reducing earmuffs can develop cracks in the colored portion of the plastic cups, posing a risk of overexposure to loud noise and sound.
- CPSCInfo
Ravin R500 Model Crossbows
If nearly but not fully cocked, the crossbow can discharge unexpectedly while consumers cock or uncock the crossbow, posing an injury hazard.
- NHTSAWarning
2023–2024 Ford Bronco
A malfunctioning child safety lock that allows a rear door to be opened unintentionally can increase the risk of injury.
- CPSCCritical
Awesafe Biometric Gun Safes
The biometric lock on the safes can fail and be opened by unauthorized users, posing a serious injury hazard and risk of death.
- CPSCInfo
Scout Kid's Bike Helmets
See the agency notice for the hazard description.
2023 (11)
- CPSCWarning
Wet & Forget "Xtreme Reach" Outdoor Rapid Application Moss, Mold, Mildew & Algae Stain Remover with Hose End Nozzle
The hose end nozzle clip can dislodge and allow the cleaning solution to spray on users, posing a risk of skin and eye irritation and other injuries.
- CPSCInfo
Squids 3705 Wire Tool Attachments - Screw Gate Tool Tail
The wire tool attachment can break when dropped while tethered to a tool exceeding two pounds, posing an injury hazard to bystanders.
- CPSCInfo
Bugaboo Dragonfly Seat Strollers
In "parent-facing" mode, the backrest of the seat can move downward, placing the infant in a negative recline. In this situation, an unrestrained infant could tumble from the seat, posing an injury hazard.
- CPSCWarning
Polaris Snowmobiles, Model Year 2022 PATRIOT 850 MATRYX RMK, INDY and SWITCHBACK
The ring gear on the primary clutch can fail, causing the clutch assembly components to come loose, posing an injury hazard to consumers.
- CPSCInfo
Model Year 2023 PATRIOT 9R MATRYX PRO RMK and PATRIOT 9R MATRYX RMK KHAOS Snowmobiles
The primary (drive) clutch can fail and can cause the clutch or clutch components to come loose, posing an injury hazard to consumers.
- CPSCInfo
Balloon Time Mini Helium Tanks
Compressed helium from the tank can escape and cause the plastic cap to be released into the air unexpectedly, posing an injury hazard due to projectiles striking users and bystanders.
- CPSCInfo
MI 1615 and 1617 Sliding Glass Doors; Window World 4000 Series and 8000 Series Sliding Glass Doors
The glass can separate from the frame during hurricane conditions which can pose a serious injury hazard.
- CPSCCritical
Biometric Gun Safes
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
- NHTSAWarning
2023–2024 Alfa Romeo Tonale
Failure to alert pedestrians when backing up increases the risk of injury.
- CPSCInfo
Residential 300 Series Snow Blowers
The recalled 300 series snow blowers can unexpectedly go into drive mode and collide with a consumer, posing an injury hazard.
- CPSCInfo
Poseidon M28A Dive Computers
The recalled Poseidon M28A Dive Computers can stop working due to intake of water causing a malfunctioning depth sensor resulting in a loss of dive data for the diver, posing an injury hazard.