Amgen, Inc.: Corlanor (ivabradine) Tablets, 5 Mg
Amgen is recalling Corlanor (ivabradine) 5 mg tablets in 14-tablet and 60-tablet bottles nationwide because a foreign substance was found in some packages. The medication is used to treat heart conditions and is available by prescription only. The recall affects all U.S. states and the District of Columbia.
- Recalling firm
- Amgen, Inc.
- Product
- Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles (NDC 55513-800-60), Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy.
- Reason
- Presence of Foreign Substance.
- Classification
- Class II
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-04
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide within the United States
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/4de58d9d-84c3-4f4d-a8a6-3725dec134f3