Drug recall
Source Plasma
FDA recall event 29185 · Class II · Aventis Bio-Services, Inc
Key facts
| Event ID | 29185 |
|---|---|
| Recall numbers | B-1701-4 |
| Recalling firm | Aventis Bio-Services, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| 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 illegal drug use, were distributed. |
| Initiation date | Nov 21, 2001 |
| City | Saint Paul |
| Country | United States |
| FEI number | 2171832 |
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