Procrit — Class II drug recall D-093-2013
Terminated recall by Physicians Total Care, Inc., reported 2012-12-26, distributed in CA, PA. Presence of Particulate Matter: glass delamination
| Recall number | D-093-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Physicians Total Care, Inc., Tulsa, OK, United States |
| Recall initiated | 2010-10-04 |
| Classified | 2012-12-14 |
| Reported by FDA | 2012-12-26 |
| Terminated | 2013-05-07 |
| Distributed | CA, PA |
| Quantity | 20 vials |
| Reason classes | foreign material, specification failure |
| NDC | 54868-5673-01 |
| Lot numbers | 05/11, 09/10, 09/12, 10/12, 11/11, 12/12, 44TK, 4NQE, 4WKN, 5KZT, 5RCM, 5RZN, 5Y8Y, 60E2 |
Product
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-093-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.