McKesson Skin Protectant recalled over manufacturing violations
- Recall date
- August 27, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- DermaRite Industries, LLC recalls McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distribu…
- Recall number
- D-0171-2026
- FDA classification
- Class II
- Brand / firm
- DermaRite Industries, LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
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