FDA recall D-0171-2026

DermaRite Industries, LLC · Class II · drug

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.

Reason for recall

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Distribution

Nationwide in the USA

Key facts

Status
Ongoing
Initiation date
2025-08-27
Report date
2025-11-26
Voluntary/Mandated
Voluntary: Firm initiated
Location
North Bergen, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0171-2026