US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Jun 4, 2026 (3 months ago)

Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Substance.

What was recalled

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

Recalling firm
Amgen, Inc.
NDC code
55513-810-60
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0615-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.