Amgen, Inc.: Corlanor (ivabradine) Tablets, 7.5mg, 60-count Bottles
Corlanor Recall Summary Amgen is recalling Corlanor (ivabradine) 7.5mg tablets in 60-count bottles nationwide because a foreign substance was found in the medication. The recall affects all U.S. states and Washington, DC. Corlanor is a prescription heart medication used to reduce heart rate in certain heart failure patients.
- Recalling firm
- Amgen, Inc.
- Product
- Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60
- 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/8ac7c6d8-8485-4433-9c23-09b2c4480f88