DermaRite recalls San-E-Foam alcohol products due to contamination at shared manufacturing facility. Affected lots produced before August 2027. Consumers should check NDC 61924-107-34 for details.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling San-E-Foam alcohol products because they were made at a facility that contaminated other products. This means the alcohol could contain harmful substances that might cause health issues if used.
The products were manufactured at a facility that previously had contamination issues. This means the alcohol could contain harmful substances that might cause health problems if used improperly.
People who own San-E-Foam alcohol products with NDC 61924-107-34 manufactured before August 2027 are affected. Those using the product for medical purposes may be at higher risk due to potential contamination.
Check for the NDC code 61924-107-34 on the product label. The product was made at DermaRite Industries LLC in North Bergen, NJ and expires by August 2027.
Look for the NDC code 61924-107-34 on the San-E-Foam product label.
The recall is due to contamination at a shared manufacturing facility, but the product is not immediately dangerous. Consumers should check if they have the affected lot and follow the recall instructions.
The recall does not specify a remedy, so you should check the product label for the NDC code 61924-107-34 and contact DermaRite if you have the affected product.
Look for the NDC code 61924-107-34 on the product label. The product was manufactured by DermaRite Industries LLC in North Bergen, NJ and expires by August 2027.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0176-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0176-2026 from DermaRite. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
