Perrigo Company PLC recalls up&up allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/antihistamine, packaged as a) 15 count bottle, NDC
Recalled January 12, 2022 · FDA recall D-0351-2022 · Perrigo Company
Hazard
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing. · FDA Class II
Units
7,272 containers
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Product
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,
Manufacturer(s)
Perrigo Company PLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →