Drug recall
Platelet Pheresis
FDA recall event 32375 · Class II · American Red Cross, Penn Jersey
Key facts
| Event ID | 32375 |
|---|---|
| Recall numbers | B-1787-5 |
| Recalling firm | American Red Cross, Penn Jersey |
| Product type | Biologics |
| Products | Platelet Pheresis |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was not prepared in accordance with acceptable specifications, was distributed. |
| Initiation date | Nov 1, 2000 |
| Termination date | Aug 1, 2005 |
| City | Philadelphia |
| Country | United States |
| FEI number | 2573021 |
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