Drug recall
Source Plasma
FDA recall event 27801 · Class III · Aventis Bioservices
Key facts
| Event ID | 27801 |
|---|---|
| Recall numbers | B-0414-4 |
| Recalling firm | Aventis Bioservices |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor whose arm inspection was not documented, was distributed. |
| Initiation date | Aug 6, 2002 |
| Termination date | Jan 20, 2004 |
| City | Flint |
| Country | United States |
| FEI number | 1000115632 |
At a glance
- 1–9 Products in this recall
- 1–9 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