Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
McKesson Skin Protectant Recalled by DermaRite Industries, LLC Due to CGMP Deviation; manufactured at the same facility where...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact DermaRite Industries, LLC directly.
Affected Products
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.
Quantity: 5,876 units
Why Was This Recalled?
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About DermaRite Industries, LLC
DermaRite Industries, LLC has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report