Procrit (epoetin alfa) injection, 20000 units/mL, 4 mL vial; Mfg By: Amgen Inc., Thousand Oaks, CA 91320; Dist. By: Physicians Total Care, Tulsa, OK 74146; NDC 54868-5673-1.
Reported: December 26, 2012 Initiated: October 4, 2010 #D-093-2013
Product Description
Procrit (epoetin alfa) injection, 20000 units/mL, 4 mL vial; Mfg By: Amgen Inc., Thousand Oaks, CA 91320; Dist. By: Physicians Total Care, Tulsa, OK 74146; NDC 54868-5673-1.
Reason for Recall
Presence of Particulate Matter: glass delamination
Details
- Recalling Firm
- Physicians Total Care, Inc.
- Units Affected
- 20 vials
- Distribution
- PA, CA
- Location
- Tulsa, OK
Frequently Asked Questions
What product was recalled? ▼
Procrit (epoetin alfa) injection, 20000 units/mL, 4 mL vial; Mfg By: Amgen Inc., Thousand Oaks, CA 91320; Dist. By: Physicians Total Care, Tulsa, OK 74146; NDC 54868-5673-1.. Recalled by Physicians Total Care, Inc.. Units affected: 20 vials.
Why was this product recalled? ▼
Presence of Particulate Matter: glass delamination
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 26, 2012. Severity: Moderate. Recall number: D-093-2013.
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