D-0171-2026 Class II Ongoing
FDA drug recall D-0171-2026 was initiated by DermaRite Industries, LLC on August 27, 2025 and is designated Class II. Reason for recall: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. The recall status is ongoing. Affected quantity: 5,876 units.
Recall Details
- Product Type
- Drugs
- Report Date
- November 26, 2025
- Initiation Date
- August 27, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 5,876 units
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.
Distribution Pattern
Nationwide in the USA
Code Information
All lots on or before expiry date 08/2027