Golden State Medical Supply Inc. recalls Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30
Recalled July 17, 2019 · FDA recall D-1462-2019 · Golden State Medical Supply
Hazard
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products. · FDA Class II
Units
4,037 bottles (121,110 tablets)
Sold at
US Nationwide One (1) US government account. No foreign accounts.
Description
CGMP Deviations: impurity for N-Nitroso-N-methyl-4-aminobutyric acid (NMBA) detected in the active pharmaceutical ingredient (API) used to manufacture finished products.
Product
Losartan Potassium, 50 mg tablets, 30 count bottle, NDC 60429-317-30
Manufacturer(s)
Golden State Medical Supply Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →