FDAHealthAugust 27, 2025
DermaRite Industries, LLC — Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side
⚠️ CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Is this relevant to me?
- Geography
- Nationwide
- Source agency
- FDA
- Category
- Health
- Published
- August 27, 2025
Nationwide in the USA
What's affected?
- Product
- Hand-E-Foam, Benzethonium Chloride 0.20%, packaged in a) 236mL (NDC 61924-102-08) and b) 1000 mL (NDC 61924-102-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
- Lot code
- on
Additional details
All lots on or before expiry date 08/2027
What should I do?
Recommended action
Class II recall. Voluntary: Firm initiated Quantity affected: 576 containers.
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