Enforcement Report - Week of December 5, 2012
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Product Detail
| Product Description | Source Plasma |
|---|---|
| Recall Number | B-0089-13 |
| Classification | Class III |
| Code Info | 07OUTF1661; 07OUTF2092; 07OUTF3219; 08OUTF2071; 08OUTF4413; 08OUTF5051; 08OUTF5772; 08OUTF6290; 08OUTF6931; 07OUTF4170; 07OUTF4787; 2473; 08OUTF7761; 08OUTF8282 |
| Product Distributed Qty | 14 units |
| Reason For Recall | Blood products, which were collected from a donor in which donor suitability were not adequately determined, were distributed. |
Event Detail
| Event Id | 48247 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | BioLife Plasma Services L.P. |
| City | Ogden |
| State | UT | Country | US |
| Voluntary / Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2008-04-17 |
| Initial Firm Notification of Consignee or Public | FAX |
| Distribution Pattern | CA |
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