Drug recall
Source Plasma
FDA recall event 32713 · Class II · Biomat USA, Inc.
Key facts
| Event ID | 32713 |
|---|---|
| Recall numbers | B-1911-5 |
| Recalling firm | Biomat USA, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for viral markers, but were collected from an ineligible donor due to behavior to increase risk of infection with human immunodeficiency virus (HIV), were… |
| Initiation date | Apr 8, 2005 |
| Termination date | Aug 29, 2005 |
| City | Wilmington |
| Country | United States |
| FEI number | 1720702 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports