Recalls / Active ingredient / Epoetin
Epoetin
2 FDA drug recalls involving the active ingredient “Epoetin”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2017-09-13 | Class II | Procrit (epoetin alfa), 10,000 units/mL, packaged in a) box of 6 single use 1 mL vials (NDC 59676-310-01), b) | Amgen, Inc. |
| 2017-08-04 | Class II | Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manuf | Amgen, Inc. |