# FDA recall D-0945-2017

> **G & W  Laboratories, Inc.** · Class III · drug recall initiated 2017-06-02.

## Product

G & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), b) 30 g tube (NDC 0713-0656-31, c) 45 g tube (NDC 0713-0656-37), d) 60 g tube (NDC 0713-0656-60), Rx Only, Manufactured by G & W Laboratories, Inc. 111 Coolidge Street, South Plainfield, NJ 07080

## Reason for recall

Failed impurities/degradation specifications: This product is being recalled due to out of specification results for Clobetasol Related Compound A, a known impurity which is a degradation product.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0945-2017
- **Recalling firm:** G & W  Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-06-02
- **Report date:** 2017-07-12
- **Termination date:** 2018-05-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** South Plainfield, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0945-2017

## Citation

> AI Analytics. FDA recall D-0945-2017. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0945-2017. Source: US FDA. Licensed CC0.

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