Enforcement Report - Week of December 5, 2012
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Product Detail
| Product Description | Source Plasma |
|---|---|
| Recall Number | B-0088-13 |
| Classification | Class II |
| Code Info | 07OUTE7481; 07OUTE6595; 07OUTE5995; 07OUTE5440; 07OUTE3268; 07OUTE2865; 07OUTE1483; 07OUTE1041; 07OUTD9210; 07OUTD8745; 07OUTD8184; 07OUTD7577; 07OUTD6988; 07OUTD6075; 07OUTD5854; 07OUTD0584; 07OUTC7070; 07OUTC6440; 07OUTC1645; 07OUTC2199; 07OUTC3461; 07OUTC3772; 07OUTC4978; 07OUTC5334; 07OUTC5999 |
| Product Distributed Qty | 25 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 | 47971 |
|---|---|
| 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 | 2008-03-07 |
| Initial Firm Notification of Consignee or Public | FAX |
| Distribution Pattern | CA |
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