← FDA ENFORCEMENT
D-0615-2026Class II

Amgen, Inc.

Recalling firm
Amgen, Inc.
Product type
Drug
Status
Ongoing
Report date
2026-07-01
Distribution
Nationwide within the United States
Firm state
CA
Product quantity
N/A
Initiated by
Voluntary: Firm initiated
Reason for recall

Presence of Foreign Substance.

Product description

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

Code / lot info

Lot #: 1138203, 1142065, Exp. Date 07/31/2026; 1145151, 1145152, 1145153, Exp. Date 2/28/2027; 1148908, 1148909, Exp. Date 05/31/2027; 1162845, 1162846, Exp. Date 11/30/2027; 1166471, 1166472, 1166473, Exp. Date 05/31/2028; 1170615, Exp. Date 08/31/2028

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.