Enforcement Report - Week of September 12, 2012
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Product Detail
| Product Description | Recovered Plasma |
|---|---|
| Recall Number | B-2440-12 |
| Classification | Class III |
| Code Info | 011FL31346, 011FL31353, 011FL31376, 011GG39708, 011GK83777, 011GN80908, 011GN80912, 011GN80914, 011GN80919, 011GN80937, 011GN80938, 011GN80941, 011GN80946, 011GN80949, 011GQ72540, 011GQ72541, 011GQ72545, 011GQ72547, 011GQ72548, 011GR66347, 011GR66349, 011GR66353, 011GR66357, 011GR66359, 011GR66361, 011GR66362, 011GR66363, 011GR66387 |
| Product Distributed Qty | 28 units |
| Reason For Recall | Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed. |
Event Detail
| Event Id | 40074 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | American National Red Cross (The) |
| City | Saint Louis |
| State | MO | Country | US |
| Voluntary / Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2005-04-15 |
| Initial Firm Notification of Consignee or Public | |
| Distribution Pattern | MO, IL, TN, AR, AL, PR, SC |
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