Enforcement Report - Week of December 12, 2012
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Product Detail
| Product Description | Source Plasma |
|---|---|
| Recall Number | B-0160-13 |
| Classification | Class III |
| Code Info | TQ192038 |
| Product Distributed Qty | 1 unit |
| Reason For Recall | Blood product, collected from a donor for whom donor suitability was not adequately determined, was distributed. |
Event Detail
| Event Id | 63435 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | Knoxville Plasma Corporation |
| City | Knoxville |
| State | TN | Country | US |
| Voluntary / Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2012-09-10 |
| Initial Firm Notification of Consignee or Public | |
| Distribution Pattern | California |
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