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Recall Observatory FDA recall evidence

Drug product

Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

D-0170-2026

August 27, 2025

Class II

Product summary

Firm
DermaRite Industries, LLC
Event
Event 97625
Status
Ongoing
Classification
Class II
Quantity
57,837 units
Official record key
drug-enforcement:D-0170-2026

Official wording

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

Code information: All lots on or before expiry date 08/2027

Distribution pattern: Nationwide in the USA

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviation