Boehringer Ingelheim Pharmaceuticals, Inc. recalls Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by: B
Recalled June 9, 2021 · FDA recall D-0600-2021 · Boehringer Ingelheim Pharmaceuticals
Hazard
Subpotent Drug · FDA Class II
Units
15,198 bottles (30 tablets per bottle)
Sold at
AR, CO, CT, LA, NC, ND, NH, NJ, OH, PA and PR
Description
Subpotent Drug
Product
Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877
Manufacturer(s)
Boehringer Ingelheim Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →