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
Reported: June 9, 2021 Initiated: May 4, 2021 #D-0600-2021
Product Description
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
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- Boehringer Ingelheim Pharmaceuticals, Inc.
- Units Affected
- 15,198 bottles (30 tablets per bottle)
- Distribution
- AR, CO, CT, LA, NC, ND, NH, NJ, OH, PA and PR
- Location
- Ridgefield, CT
Frequently Asked Questions
What product 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. Recalled by Boehringer Ingelheim Pharmaceuticals, Inc.. Units affected: 15,198 bottles (30 tablets per bottle).
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 9, 2021. Severity: Moderate. Recall number: D-0600-2021.
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