Enforcement Report - Week of September 12, 2012
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Product Detail
| Product Description | Source Plasma |
|---|---|
| Recall Number | B-2370-12 |
| Classification | Class III |
| Code Info | 380001943, 380002525, 380004157, 380005454, 380006271, 380007553, 380007713, 380002110. 380001521, 380003365, 380003625, 380005713, 380006093, 380008037, 380008629, 380008896, 380009446, 380009942, 380010141, 380010432, 380010668, 380011122, 380011476, 380012030, 380012185, 380012470, 380012689, 380013021, 380013200, 380013643, 380013915, 380014838, 380015927, 380016011, 380016486. |
| Product Distributed Qty | 35 units |
| Reason For Recall | Blood products, collected from a donor, whose suitability to donate was not adequately determined, were distributed |
Event Detail
| Event Id | 39858 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | Biomat USA, Inc. |
| City | Los Angeles |
| State | CA | Country | US |
| Voluntary / Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2005-03-08 |
| Initial Firm Notification of Consignee or Public | Letter |
| Distribution Pattern | all units were shipped to Spain |
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