Reported Jul 1, 2026 · Ongoing · Updated Sep 16, 2026

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC 55513-800-99), and b) 60 tablet bottles…

Amgen, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Amgen, Inc. · 1 Amgen Center Dr · Thousand Oaks, CA · 91320-1730

Is this the product you have?

  • 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.
Lot codes and dates
  • 72 of 72 codes

    • a) Lot # 1138901
    • Exp. Date 08/31/2026
    • 1149846
    • Exp. Date 04/30/2027 b) Lot #1138201
    • 1138202
    • 08/31/2026
    • 1138900
    • 1141143
    • Exp. Date 08/31/2026
    • 1140280
    • 1140281
    • 1142063
    • Exp. Date 10/31/2026
    • 1142062
    • 1142942
    • 1142943
    • Exp. Date 11/30/2026
    • 1144081
    • 1144104
    • Exp. Date 12/31/2026
    • 1146373
    • 1146374
    • Exp. Date 01/31/2027
    • 1147491
    • 1147492
    • 1149843
    • Exp. Date 03/31/2027
    • 1151113
    • 1151890
    • 1153401
    • Exp. Date 07/31/2027
    • 1151114
    • 1151115
    • Exp. Date 09/30/2027
    • 1152412
    • 1153399
    • 1153400
    • Exp. Date 06/30/2027
    • 1155834
    • 1155835
    • Exp. Date 04/30/2027
    • 1155836
    • Exp. Date 09/30/2027
    • 1158480
    • 1158481
    • 1158482
    • Exp. Date 10/31/2027
    • 1160354
    • 1160355
    • Exp. Date 03/31/2028
    • 1161593
    • 1161594
    • 1161595
    • Exp. Date 04/30/2028
    • 1164097
    • 1164098
    • 1164099
    • Exp. Date 06/30/2028
    • 1165078
    • 1165079
Amount recalled
934577 bottles

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

Presence of Foreign Substance.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 5:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.