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

allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count…

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

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-count cartons (NDC 11673-617-39), c)70-count cartons (NDC 11673-617-01), and d)150-count cartons (11673-617-47), Distributed by: Target Corporation, Minneapolis, MN 55403.

Recalling firm
L. Perrigo Company
NDC code
11673-617-22
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0910-2023

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.

Other Chloride recalls

See all