Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Int
See all recalls from Amgen, Inc. →Recalled Product
Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320-1799, Manufactured for: Janssen Products, LP Horsham, PA 19044, NDC 59676-340-01
Hazard / Issue
Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: G290491A, G290491B, Exp. 06/18
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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