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High risk Drugs & MedicationsClass II

Corlanor Ivabradine 7.5mg Recall

Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60

Updated June 4, 2026

Corlanor (ivabradine) 7.5mg tablets in 60-count bottles are being recalled due to the presence of a foreign substance. If you take this medication, stop and contact your pharmacy or doctor immediately.

Is the Amgen, Inc. recalled? Yes. This product was recalled by FDA on June 4, 2026. Details below.

What is recalled

Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, NDC 55513-810-60, manufactured by Amgen Inc. (Thousand Oaks, CA), made in Italy.

Am I affected

You're affected if you have a 60-count bottle of Corlanor 7.5mg tablets with NDC number 55513-810-60 in your possession.

What to do right now

Stop taking this medication immediately. Contact your pharmacy or prescribing doctor right away to discuss your current supply and get a replacement or alternate treatment.

The hazard

Presence of Foreign Substance.

Brands affected

Amgen, Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0615-2026
Classification
Class II
Recalled
June 4, 2026
Read the official notice

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