Amgen, Inc. recalls Procrit Epoetin Alfa 40,000 units/mL single use vial For Intravenouse or Subcutaneous Use Only, Rx only, Manufactured by
Recalled August 23, 2017 · FDA recall D-1086-2017 · Amgen
Hazard
Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials. · FDA Class II
Units
175,632 vials
Sold at
United States including Puerto Rico
Description
Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.
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
Manufacturer(s)
Amgen, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →