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Serious recall: Injury is possible or has been reported. Take action promptly.

Amgen, Inc. 2026-07-01 Health serious FDA
Health · FDA · Recall #FDA-D-0612-2026

Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC… Recall

Issued July 1, 2026 · Amgen, Inc.

In July 2026, Amgen, Inc. recalled the Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC…, a serious health recall reported by the FDA.

Compiled by Dana Whitfield, RecallCheckr

What this means for you

Presence of Foreign Substance.

What you should do

  1. 1 Stop using Corlanor (ivabradine) tablets, 5 mg, packaged in a) 14 tablets bottles (NDC… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Amgen, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Amgen, Inc.
Category
Health
Recall date
July 1, 2026
Units affected
Not reported
Sold at
Nationwide within the United States
Recall number
FDA-D-0612-2026
Made in
United States
Issuing agency
FDA

In context

  • Amgen, Inc. has 4 recalls in our database.
  • We're tracking 3,673 Health recalls in our database.
  • This is the 453rd Health recall we've logged in 2026.
Read the official FDA notice

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