US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 28, 2019 (7 years ago)

AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per…

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

Why it was recalled

Failed Stability Specifications.

What was recalled

AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per bottle, NDC 42291-297-50.

Recalling firm
AVKARE Inc.
NDC code
42291-297-50
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1875-2019

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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