Drug recall
Source Plasma
FDA recall event 30927 · Class II · Alpha Therapeutic Corporation
Key facts
| Event ID | 30927 |
|---|---|
| Recall numbers | B-0669-5 |
| Recalling firm | Alpha Therapeutic Corporation |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for antibodies to human immunodeficiency virus, types 1 and 2 (anti-HIV- 1/2), but were collected from a donor that subseqently reported a previous reactive test… |
| Initiation date | May 8, 2003 |
| Termination date | Feb 22, 2005 |
| City | San Antonio |
| Country | United States |
| FEI number | 1000118834 |
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