Drug recall
Source Plasma
FDA recall event 29070 · Class II · Biomat USA
Key facts
| Event ID | 29070 |
|---|---|
| Recall numbers | B-1591-4 |
| Recalling firm | Biomat USA |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed |
| Initiation date | Feb 18, 2004 |
| City | Hampton |
| Country | United States |
| FEI number | 3003832406 |
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