Is PROCRIT (epoetin alfa) injection, 10,000 Units/mL, 1 mL Single-Use Vial (NDC 59676-310-00); packaged in a) 6 x 1 mL Single Use Vials per carton (NDC 59676-310-01, packed in 4 cartons per tray; b) 25 x 1 mL Single Use Vials per carton (NDC 59676-310-02); Rx only; Manufactured by: Amgen Inc., U.S. License #1080, One Amgen Center Drive, Thousand Oaks, California 91320-1799; Distributed by: Ortho Biotech Products, L.P., Raritan, New Jersey 08869-0670. recalled?

Question

Accepted Answer

Presence of Particulate Matter: This is an extension of the Procrit recall initiated on September 22, 2010  and extended on October 13, 2010 due to extremely thin glass flakes that have the potential to be present in Procrit. (epoetin alfa) vials.

Distribution: Nationwide

Centocor Ortho Biotech Services LLC: Presence of Particulate Matter: This is an extension of the Procrit recall initiated on September 22, 2010 and extended on October 13, 2010 due to extremely thin glass flakes that have the potential to be present in Procrit. (epoetin alfa) vials.

Additional Information

Were You Affected by This Recall?

Centocor Ortho Biotech Services LLC: Presence of Particulate Matter: This is an extension of the Procrit recall initiated on September 22, 2010 and extended on October 13, 2010 due to extremely thin glass flakes that have the potential to be present in Procrit. (epoetin alfa) vials.

Additional Information

Were You Affected by This Recall?