US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 17, 2022 (4 years ago)

Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.

What was recalled

Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube, Rx Only, Manufactured By Perrigo, Bronx, NY 10457, Distributed By Perrigo, Allegan, MI 49010, NDC 45802-064-36.

Recalling firm
Padagis US LLC
NDC code
45802-064-36
Origin
MN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1497-2022

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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