Amgen, Inc. recalls Corlanor
- Recalling company
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Jun 4, 2026
- Reported
- Jul 1, 2026
- Distribution
- Nationwide within the United States
- Status
- Ongoing
- Quantity
- N/A
- Lot / codes
- Lot #: 1138203, 1142065, Exp. Date 07/31/2026; 1145151, 1145152, 1145153, Exp. Date 2/28/2027; 1148908, 1148909, Exp. Date 05/31/2027; 1162845, 1162846, Exp. Date 11/30/2027; 1166471, 1166472, 1166473, Exp. Date 05/31/2028; 1170615, Exp. Date 08/31/2028
- Company location
- Thousand Oaks, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0615-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0615-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.