Drug recall
Platelet Pheresis, Leukoreduced
FDA recall event 29029 · Class III · American Natl Red Cross Mid At
Key facts
| Event ID | 29029 |
|---|---|
| Recall numbers | B-1604-4, B-1605-4 |
| Recalling firm | American Natl Red Cross Mid At |
| Product type | Biologics |
| Products | Platelet Pheresis, Leukoreduced, Platelet Pheresis, Leukoreduced, Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood Products, incorrectly tested for syphilis, were distributed. |
| Initiation date | Feb 25, 2004 |
| Termination date | Jul 22, 2004 |
| City | Norfolk |
| Country | United States |
| FEI number | 1173024 |
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