A hospital operating room with medical equipment (representative file photo). Specific recalled device: see recall details below. Photo: FDA / Public Domain.
Recall Database
Other Injury Hazards Recalls
This is the catch-all hub — 115 records that don't fall cleanly into one of the named hazard classes. The mix is 80 FDA, 28 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, kept small so the named hubs stay clean.
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 through 2026, weighted toward 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 115 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); a record can carry secondary hazard tags but appears on only one hub. Regulators in this hub: FDA (80), CPSC (28), 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 captured through late May 2026 (CPSC and NHTSA refreshed May 27, FDA May 28, 2026), and it grows as new notices are ingested. Every row links to the original agency notice. The agency's record is the authority; the hazard grouping is ours.
2026 (65)
- 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
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are
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
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
2024 Toyota Corolla Cross Hybrid
Insufficient pedestrian warning sounds may fail to alert pedestrians of a reversing vehicle, increasing the risk of injury.
- 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 (6 fl oz cups
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 (6 fl oz cups
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
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
Booey's Dragon's Breath sauce
Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.
- 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
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
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
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
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
VACUUM BAG SU LARGE
There is a possibility of reagent leakage from the specimen container.
- 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 issue that renders the touch screen unresponsive.
- FDAClass II
Divided Sunset Multi Collagen Peptides
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 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
Presence of Thiamethoxam-PESTICIDE
- FDAClass II
Isotretinoin Capsules
Superpotent and Subpotent
- FDAClass II
Isotretinoin Capsules
Superpotent and Subpotent
- FDAClass II
Mint Lesion
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 (25)
- 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! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)
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)
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
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
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
elevated levels of aflatoxin
- NHTSAWarning
2024 BMW X3
Doors that can be inadvertently unlocked and unlatched may open unexpectedly, increasing the risk of injury to rear seat occupants.
2024 (16)
- 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 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
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
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.
2023 (9)
- 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.
- 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
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.