Recalls / Class II
Class IID-0171-2026
Product
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.
- Brand name
- Skin Protectant With Lanolin
- Generic name
- Lanolin
- Active ingredient
- Lanolin
- Route
- Topical
- NDCs
- 68599-6202, 68599-6203
- FDA application
- M016
- Affected lot / code info
- All lots on or before expiry date 08/2027
Why it was recalled
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Recalling firm
- Firm
- DermaRite Industries, LLC
- Manufacturer
- McKesson Medical-Surgical Inc.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 7777 W Side Ave, North Bergen, New Jersey 07047-6436
Distribution
- Quantity
- 5,876 units
- Distribution pattern
- Nationwide in the USA
Timeline
- Recall initiated
- 2025-08-27
- FDA classified
- 2025-11-20
- Posted by FDA
- 2025-11-26
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0171-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.