Amgen, Inc. recalls
Every recall we track for Amgen, Inc. — 12 in all, from 2013–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
10 recalls since 2017. 10% rated “stop using now”.
All FDA recall records for Amgen, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 1 | 0 | 0 | 1 | 2 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 2 | 0 | 2 |
| 2026 (to date) | 0 | 0 | 1 | 4 | 5 |
Amgen, Inc. recalls before 2017
Recalls on record by year.
Most common reasons for Amgen, Inc. recalls
What to do if you have a recalled Amgen, Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Amgen, Inc. recalls
7 shown- UnratedDrug
Amgen, Inc. recalls Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC
Amgen recalls 7.5mg Corlanor tablets with foreign substance. Affected lots expire through 2028. No remedy specified in recall notice.
AmgenJun 4, 2026 - Lower riskDrug
Amgen, Inc. recalls Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use
Amgen recalls Neupogen (filgrastim) vials that may lose potency before their 36-month expiry date. This could affect medication effectiveness if used after the stability period ends.
AmgenFeb 27, 2025 - Use cautionDrug
Amgen, Inc. recalls MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only,
Amgen recalls MVASI (bevaciz:awwb) injections due to potential container leaks. This risk affects patients receiving the drug for cancer treatment. Contact Amgen for details.
AmgenMay 2, 2022 - UnratedDrug
Amgen, Inc. recalls Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) box of 25
Amgen recalls Procrit (epoetin alfa) 10,000 units/mL vials due to glass flakes found during quality checks. Affected lots expire July 2018. No remedy specified in recall notice.
AmgenSep 13, 2017 - Stop using nowDrug
Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured
Amgen recalls Procrit Epoet: 40,000 units/mL vials with visible glass flakes that could cause injury during injection. Check NDC 59676-340-01, lots G290491A/B, expiring 06/18.
AmgenAug 4, 2017 - Stop using nowDrug
Amgen, Inc. recalls AMGEN Kyprolis (carfilzomib) for injection, 30 mg per vial, Discard unused portion, For Intravenous Administration
Amgen recalls Kyprolis (carfilzom: 30mg vials) due to potential glass cracks that could allow contamination. Discard unused portions immediately. This is for intravenous use only.
AmgenDec 15, 2016 - Use cautionDrug
Amgen, Inc. recalls Prolia (denosumab) Injection, 60 mg/mL, 1 x 60 mg Single Use Prefilled Syringe per carton, Rx only, Manufactured by:
Amgen recalls specific lots of Prolia (denosumab) prefilled syringes due to visible cellulose fibers. Check your lot number and expiration date for details.
AmgenSep 17, 2013
Amgen, Inc. recall questions
How many recalls has Amgen, Inc. had?
12 recalls from Amgen, Inc. are on record with U.S. safety agencies, from 2013–2026.
What is the most recent Amgen, Inc. recall?
Amgen, Inc. recalls Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC, dated Jun 4, 2026. Every Amgen, Inc. recall is listed on this page, newest first.
Why are Amgen, Inc. products recalled?
The most common reasons on record: CGMP Deviations (3); Presence of Foreign Substance. (2).
What should I do if I have a recalled Amgen, Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Amgen, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.