Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

G & W Fluocinolone Acetonide Cream USP 0.025% Recalled by G & W Laboratories Inc Due to Failed Content Uniformity Specifications; at the 18 month...

Date: September 30, 2013
Company: G & W Laboratories Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact G & W Laboratories Inc directly.

Affected Products

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

Quantity: 187,368 metal tubes

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About G & W Laboratories Inc

G & W Laboratories Inc has 1 total recall tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report