WhichRecall
Class IIReported 2025-11-26

San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-107-34

Recalled by DermaRite Industries, LLC

Reason for Recall

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

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Recall Number
D-0176-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-08-27
Reported
2025-11-26
Distribution
Nationwide in the USA
Code Info
All lots on or before expiry date 08/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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