Drug recall
Source Plasma
FDA recall event 29115 · Class III · Aventis Behring
Key facts
| Event ID | 29115 |
|---|---|
| Recall numbers | B-1504-4 |
| Recalling firm | Aventis Behring |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was collected from a donor in which the arm inspection was not performed prior to phlebotomy, was collected. |
| Initiation date | Apr 22, 2002 |
| Termination date | Jul 13, 2004 |
| City | King Of Prussia |
| Country | United States |
| FEI number | 3003067005 |
At a glance
- 1–9 Products in this recall
- None 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