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Recall Observatory FDA recall evidence

Drug 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.

D-0167-2026

August 27, 2025

Class II

Product summary

Firm
DermaRite Industries, LLC
Event
Event 97625
Status
Ongoing
Classification
Class II
Quantity
576 containers
Official record key
drug-enforcement:D-0167-2026

Official wording

Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Code information: All lots on or before expiry date 08/2027

Distribution pattern: Nationwide in the USA

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviation