PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.
Class II · Ongoing
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
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Affected lots / codes — check yours against thisAll lots on or before expiry date 08/2027
- Recalling firm
- DermaRite Industries, LLC, North Bergen, NJ
- Classification
- Class II (temporary or reversible harm possible)
- Status
- Ongoing
- Quantity
- 381,619 units
- Distribution
- Nationwide in the USA
- Recall initiated
- August 27, 2025
- Classified
- November 20, 2025
- Initiation
- Voluntary: Firm initiated
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Official source. This record is published by the U.S. FDA through the openFDA
enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0173-2026%22
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0173-2026%22
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Important. Recalls target specific lots and codes — compare the affected lots
above against your own product. This page reproduces public FDA data for readability;
EveryRecall is independent and not affiliated with the FDA.
See every recall for this brand: Is DermaRite Industries, LLC recalled? →
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