US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 9, 2023 (4 years ago)

aller-ease

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

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Packaged For: Your Military Exchanges, By: Perrigo Company, Allegan, MI USA 49010. NDC 55301-847-39

Recalling firm
L. Perrigo Company
NDC code
55301-847-39
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0904-2023

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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