Enforcement Report - Week of June 20, 2012
-
Back to Previous Page
Event Detail
| Event ID | 40880 |
|---|---|
| Product Type | Biologics |
| Status | Terminated |
| Recalling Firm | Biomat USA, Inc. |
| City | Reno |
| State | NV |
| Country | US |
| Voluntary/Mandated | Voluntary: Firm Initiated |
| Recall Initiation Date | 2005-09-28 |
| Initial Firm Notification of Consignee or Public | Letter |
| Distribution Pattern | Spain |
Product Detail
| Product Description | Code Info | Classification | Reason for Recall | Product Quantity | Recall Number |
|---|---|---|---|---|---|
| Source Plasma | 0300101489, 0300100390, 0300099622, 0300098831, 0300098638, 0300098192 | Class III | Blood products collected from a donor who was permanently deferred for unsuitable test results, were distributed. | 6 | B-1475-12 |
-
