Drug recall
Source Plasma
FDA recall event 29182 · Class II · Aventis Bio-Services, Inc.
Key facts
| Event ID | 29182 |
|---|---|
| Recall numbers | B-1805-4 |
| 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, which tested initially reactive for an infectious disease on an invalidated test run but subsequently tested negative on a single repeat run, were distributed. |
| Initiation date | Feb 19, 2002 |
| City | Minneapolis |
| Country | United States |
| FEI number | 2177738 |
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