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Amgen, Inc. recall records

7 reported ongoing

8 records in this archive. Latest source date Jun 4, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

Jun 4, 2026FDA drug enforcement

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 92...

Presence of Foreign Substance.

Class IIReported ongoing

Distribution: Nationwide within the United States

Official source

Jun 4, 2026FDA drug enforcement

Sensipar (cinacalcet) Tablets, 30mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-073-30

CGMP Deviations

Class IIReported ongoing

Distribution: Nationwide within the United States

Official source

Jun 4, 2026FDA drug enforcement

Sensipar (cinacalcet) Tablets, 60mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks ,CA 91320-1799, Made in Japan. NDC 55513-074-30

CGMP Deviations

Class IIReported ongoing

Distribution: Nationwide within the United States

Official source

Jun 4, 2026FDA drug enforcement

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

Presence of Foreign Substance.

Class IIReported ongoing

Distribution: Nationwide within the United States

Official source

Jun 4, 2026FDA drug enforcement

Sensipar (cinacalcet) Tablets, 90mg, 30-count bottles, Rx Only, Distributed by: Amge, One Amgen Center Drive, Thousand Oaks, CA 91320-1799, Made in Japan. NDC 55513-075-30

CGMP Deviations

Class IIReported ongoing

Distribution: Nationwide within the United States

Official source

Feb 27, 2025FDA drug enforcement

Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No Preservative, Amgen Inc., Thou...

Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.

Class IIReported ongoing

Distribution: Nationwide in the U.S.A. and Belgium/Luxembourg, Brazil, Chile, Colombia, France/French Guiana, Germany, Ireland, Italy/San Marino, Netherlands, Poland, Spain/Andorra, Sweden, F...

Official source

Feb 27, 2025FDA drug enforcement

Neupogen (filgrastim) For Injection, 480 mcg/1.6 mL (300 mcg/1 mL), 1.6 mL single Dose Vial, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No Preservativ...

Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.

Class IIReported ongoing

Distribution: Nationwide in the U.S.A. and Belgium/Luxembourg, Brazil, Chile, Colombia, France/French Guiana, Germany, Ireland, Italy/San Marino, Netherlands, Poland, Spain/Andorra, Sweden, F...

Official source

May 2, 2022FDA drug enforcement

MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, ND...

Defective container: loose crimp defect, potential loss of container integrity.

Class IIReported terminated

Distribution: Nationwide in the USA, Egypt and Lithuania.

Official source

Reasons in these listed records

Presence of Foreign Substance.
CGMP Deviations
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Defective container: loose crimp defect, potential loss of container integrity.

These examples come from this result page and are not a ranking of every recall reason.

Checking Amgen, Inc.

Is there a recall on amgen, inc. right now?

This archive contains 8 records, including 7 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.

Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.

Where can I find older records?

Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

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