Amgen, Inc.: Corlanor (ivabradine) Tablets, 5 Mg
Corlanor (ivabradine) Recall Summary Amgen is recalling Corlanor 5 mg tablets in 14-tablet and 60-tablet bottles nationwide because a foreign substance was found in the medication. The recall affects patients across all U.S. states who received these specific bottles. This is a Class II recall, meaning the product could cause adverse health effects.
- 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/90762188-9e05-4ad9-ba76-737f6ca8ae21