Home / drug / D-0171-2026 Class II Reported 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 .