Viatris recalls Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV
Recalled September 22, 2021 · FDA recall D-0798-2021 · Viatris
Hazard
Failed Impurities/Degradation Specifications; out of specification for Related Compound · FDA Class III
Units
21,094
Sold at
Product was distributed nationwide.
Description
Failed Impurities/Degradation Specifications; out of specification for Related Compound
Product
Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 NDC 0378-3231-93
Manufacturer(s)
Viatris
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →