US Drug Recall Register
Class III · Low risk Terminated Initiated Sep 30, 2013 (13 years ago)

G & W Fluocinolone Acetonide Cream USP 0.025%, a) 15 gm (NDC 0713-0222-15), b) 60 gm (NDC…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

What was recalled

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

Recalling firm
G & W Laboratories Inc
NDC code
0713-0222-15
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-391-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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