Recall Database
Dermarite Industries Recalls
An assortment of pharmaceutical pills (representative file photo). Specific recalled product: see recall details below. Photo: Michael Nutt / Wikimedia Commons (CC BY-SA 2.0).
- Recalls in database
- 18
- Agency
- FDA
- Years covered
- 2025
- Primary hazards
- Drug & Medical Product Contamination (18)
DermaRite Industries has 18 records, all FDA recalls, and all 18 classify as drug or medical-product contamination in the site's taxonomy. Every notice was published in 2025.
This is an FDA-only, single-hazard hub. Use it to check an affected product by lot. Each row links to the FDA enforcement record with the recall classification and the firm's corrective action.
How this hub is built. This page collects the 18 recall records tied to Dermarite Industries in the current 411 Press recall dataset. Records are grouped by a normalized version of the recalling firm's name (normalizer version 2026-07-28.C3.2). Parent, subsidiary, and "doing business as" relationships are not merged unless the agency data states them, so a corporate family can appear under more than one name. Regulator for these records: FDA. They were published 2025. A recall count reflects how much recall activity fell inside the ingestion window — roughly February 2023 through May 2026, refreshed late May 2026 — not a ranking of relative safety. Larger manufacturers and higher-volume product lines file more notices. This is the current dataset, not an all-time total, and it grows as new notices are ingested. Every row links to the original agency notice.
2025 (18)
- Class II
UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
San-E-Foam, Alcohol 67%, 1000 mL (34 fl.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
Renew Skin Repair Cream
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
Renew PeriProtect
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
PeriGuard Ointment
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
PeriGiene
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
McKesson Skin Protectant
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
Lantiseptic
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
Lantiseptic
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
KleenFoam Antimicrobial Foam Soap
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
Hand-E-Foam
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
GelRite Instant Hand Sanitizer
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
DermaSarra
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
DermaKleen
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
DermaFungal
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
DermaCerin
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
- Class II
4-N-1 Skin Protectant
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.