FDA · Drugs · Wednesday, July 1

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

Quantity: N/A

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: Wednesday, July 1
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-0615-2026
Source: U.S. Food and Drug Administration

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