US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 23, 2019 (7 years ago)

fexofenadine hydrochloride tablets USP, 180 mg, 150-count bottle, Member's Mark…

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

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

fexofenadine hydrochloride tablets USP, 180 mg, 150-count bottle, Member's Mark, Distributed by: Sam's West, Inc., Bentonville, AR 22716, NDC 68196-976-91, UPC 0 78742 23550 9.

Recalling firm
Aurolife Pharma, LLC
NDC code
68196-976-91
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1867-2019

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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