Enforcement Report - Week of October 17, 2012
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Product Detail
| Product Description | Source Plasma |
|---|---|
| Recall Number | B-1996-12 |
| Classification | Class II |
| Code Info | 5080238043; 5080237145; 5080235642; 5080235128; 5080234049; 5080233479; 5080232406; 5080225818; 5080224961; 5080223129; 5080221982; 5080215743; 5080214633; 5080213587; |
| Product Distributed Qty | 14 |
| Reason For Recall | Blood products, collected from a donor whose physical examination was incomplete, were distributed. |
Event Detail
| Event Id | 62446 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | Octapharma Plasma, Inc. |
| City | Norfolk |
| State | VA | Country | US |
| Voluntary / Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2012-05-16 |
| Initial Firm Notification of Consignee or Public | |
| Distribution Pattern | Austria |
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