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.
Reported: November 26, 2025 Initiated: August 27, 2025 #D-0171-2026
Product Description
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.
Reason for Recall
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Details
- Recalling Firm
- DermaRite Industries, LLC
- Units Affected
- 5,876 units
- Distribution
- Nationwide in the USA
- Location
- North Bergen, NJ
Frequently Asked Questions
What product 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.. Recalled by DermaRite Industries, LLC. Units affected: 5,876 units.
Why was this product recalled? ▼
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0171-2026.
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