# FDA recall D-0171-2026

> **DermaRite Industries, LLC** · Class II · drug recall initiated 2025-08-27.

## 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

- **Recall number:** D-0171-2026
- **Recalling firm:** DermaRite Industries, LLC
- **Classification:** Class II
- **Product type:** drug
- **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

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

## Citation

> AI Analytics. FDA recall D-0171-2026. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0171-2026. Source: US FDA. Licensed CC0.

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