Perrigo Company PLC recalls allergyrelief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 56062
Recalled January 12, 2022 · FDA recall D-0344-2022 · Perrigo Company
Hazard
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing. · FDA Class II
Units
2280 containers
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Product
allergyrelief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 56062-571-22 UPC 0 41415 38973 1; b) 45 count bottle, NDC 56062-571-95 UPC 0 41415 38773 7; Distributed by PubliX SUpermarket Inc 3300 Publix Corporate Parkway Lakeland, FL 33811, Made in the Czech Republic
Manufacturer(s)
Perrigo Company PLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →