Perrigo Company PLC recalls Perrigo Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, 100 count bottle, Made in the Czech Republic, D
Recalled January 12, 2022 · FDA recall D-0345-2022 · Perrigo Company
Hazard
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing. · FDA Class II
Units
89,664 containers
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Product
Perrigo Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, 100 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan, MI 49010 NDC 45802-571-78 UPC 3 45802 571 78 6
Manufacturer(s)
Perrigo Company PLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →