Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hand-E-Foam Recalled by DermaRite Industries, LLC Due to CGMP Deviation; manufactured at the same facility where...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact DermaRite Industries, LLC directly.
Affected Products
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.
Quantity: 576 containers
Why Was This Recalled?
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About DermaRite Industries, LLC
DermaRite Industries, LLC has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report