FDA recall D-0173-2026

DermaRite Industries, LLC · Class II · drug

Product

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.

Reason for recall

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

Distribution

Nationwide in the USA

Key facts

Status
Ongoing
Initiation date
2025-08-27
Report date
2025-11-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
North Bergen, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0173-2026