# FDA recall D-391-2014

> **G & W  Laboratories Inc** · Class III · drug recall initiated 2013-09-30.

## Product

G & W Fluocinolone Acetonide Cream USP 0.025%, a) 15 gm (NDC 0713-0222-15), b) 60 gm (NDC 0713-0222-60 ), Rx Only, Manufactured by: G&W Laboratories, Inc. 111 Coolidge Street, South Plainfield, NJ 07080

## Reason for recall

Failed Content Uniformity Specifications; at the 18 month time point.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-391-2014
- **Recalling firm:** G & W  Laboratories Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-09-30
- **Report date:** 2014-01-08
- **Termination date:** 2014-08-28

- **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-391-2014

## Citation

> AI Analytics. FDA recall D-391-2014. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-391-2014. Source: US FDA. Licensed CC0.

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