Amgen's product recalls
4 official recall notices between Mar 2025 and Jul 2026 were matched to Amgen.
Each notice concerns the specific products, sizes and lot codes it names. A recall does not mean that other Amgen products are affected, and a count of notices is not a measure of safety: one incident can produce a notice for every pack size.
Covers only notices from the U.S. Food and Drug Administration enforcement reports (openFDA), USDA Food Safety and Inspection Service recalls, UK Food Standards Agency food alerts and U.S. Consumer Product Safety Commission recalls that could be matched to Amgen: the recalling firm must be Amgen, a parent or a subsidiary, and for a brand the brand name must appear in the product description. Method.
2026 (2)
| Date | Product | Brand | Recalling firm | Reason given | Source |
|---|---|---|---|---|---|
| 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.,… | — | Amgen, Inc. | Presence of Foreign Substance. Class II | FDA | |
| Corlanor (ivabradine) tablets, 7.5mg, 60-count bottles, Rx Only, Amgen Inc., Thousand Oaks, CA 92130 Made In Italy. NDC 55513-810-60 | — | Amgen, Inc. | Presence of Foreign Substance. Class II | FDA |
2025 (2)
| Date | Product | Brand | Recalling firm | Reason given | Source |
|---|---|---|---|---|---|
| Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials, Rx Only, For Subcutaneous or Intravenous Use Only, Sterile Solution - No… | — | Amgen, Inc. | 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 II | FDA | |
| 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… | — | Amgen, Inc. | 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 II | FDA |
Product descriptions and reasons are shortened from the regulators' own text; the linked notice is the authoritative record. See all matched recalls, or report a wrong match through the corrections page.