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)
This hub covers 1 recall event involving DermaRite Industries, published by the FDA as 18 product-line records, 2025–2025. DermaRite makes skin- and wound-care products; the FDA issues one record per affected product line, so a single recall can appear as many records.
Each row links to the FDA enforcement record with the classification and the firm's corrective action.
How this hub is built. This page collects 1 recall event tied to DermaRite Industries (across 18 product-line records) in the current 411 Press recall dataset. A note on counting. The three agencies package recalls differently. NHTSA issues one record per safety campaign; the CPSC issues one per recall; the FDA issues one per affected product line, so a single FDA recall can appear as dozens of records. Counting raw records would push FDA-heavy brands artificially to the top. The counts here are recall EVENTS — distinct agency events — with the FDA product-line record total shown alongside wherever the two differ. 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 2025–2025. An event count reflects how much recall activity fell inside the current dataset — not a ranking of relative safety. Larger manufacturers and higher-volume product lines generate more recall activity. 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
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
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, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL
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, Camphor 0.5%, External Analgesic, 222 mL
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, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL
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.