Corlanor Ivabradine 5mg Recall
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 O
Updated June 4, 2026
Corlanor (ivabradine) 5 mg tablets are being recalled because bottles may contain a foreign substance. If you take this medication, stop and contact your pharmacy or doctor right away.
Is the Amgen, Inc. recalled? Yes. This product was recalled by FDA on June 4, 2026. Details below.
What is recalled
Corlanor (ivabradine) tablets, 5 mg, in two bottle sizes: 14-tablet bottles (NDC 55513-800-99) and 60-tablet bottles (NDC 55513-800-60), manufactured by Amgen Inc. in Italy.
Am I affected
You are affected if you have a prescription bottle of Corlanor 5 mg tablets with NDC number 55513-800-99 (14 tablets) or 55513-800-60 (60 tablets).
What to do right now
Stop taking this medication immediately. Contact your pharmacy or doctor to confirm whether your bottle is affected and to get a replacement or alternative treatment.
The hazard
Presence of Foreign Substance.
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0612-2026
- Classification
- Class II
- Recalled
- June 4, 2026
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