US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 27, 2021 (5 years ago)

up&up allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/antihistamine…

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

Why it was recalled

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

What was recalled

up&up allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/antihistamine, packaged as a) 15 count bottle, NDC 11673-571-22 UPC 3 70030 62303 7; b) 30 count bottle, NDC 11673-571-39 UPC 3 70030 62301 3; Distributed by Target Corp., Mpls., MN 55403, Made in the Czech Republic,

Recalling firm
Perrigo Company PLC
NDC code
11673-571-22
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0351-2022

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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