US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 4, 2021 (5 years ago)

Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Subpotent Drug

What was recalled

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

Recalling firm
Boehringer Ingelheim Pharmaceuticals, Inc.
NDC code
0597-0041-37
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0600-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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