WhichRecall
Class IIReported 2025-11-26

McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distributed by McKesson Medical-Surgical Inc., Richmond, VA 23233.

Recalled by DermaRite Industries, LLC

Reason for Recall

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

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Recall Number
D-0171-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-08-27
Reported
2025-11-26
Distribution
Nationwide in the USA
Code Info
All lots on or before expiry date 08/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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