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FDA · Drugs ·

Corlanor (ivabradine) tablets recall

Amgen, Inc. recalled Corlanor (ivabradine) tablets on July 1, 2026 because of presence of Foreign Substance. It was sold nationwide.

Why it was recalled

Presence of Foreign Substance.

What's recalled

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.

Quantity: 934577 bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Amgen, Inc., Thousand Oaks, CA
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Nationwide within the United States
Status
Ongoing
Recall number
D-0612-2026
Source
U.S. Food and Drug Administration

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