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.
Reported: November 26, 2025 Initiated: August 27, 2025 #D-0173-2026
Product Description
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.
Details
- Recalling Firm
- DermaRite Industries, LLC
- Units Affected
- 381,619 units
- Distribution
- Nationwide in the USA
- Location
- North Bergen, NJ
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by DermaRite Industries, LLC. Units affected: 381,619 units.
Why was this product recalled? ▼
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0173-2026.
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