Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of particulate matter: glass flakes identified as...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Amgen, Inc. directly.
Affected Products
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 single use 1 mL vials (NDC 59676-310-02), Rx Only, Manufactured by: Amgen, Inc. Thousand Oaks, CA 91320, Manufactured for: Janssen Products, LP Horsham, PA 19044
Quantity: 275,380 vials
Why Was This Recalled?
Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Amgen, Inc.
Amgen, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report