Drug recall
Platelets Pheresis
FDA recall event 30542 · Class III · Delta Blood Bank
Key facts
| Event ID | 30542 |
|---|---|
| Recall numbers | B-0395-5 |
| Recalling firm | Delta Blood Bank |
| Product type | Biologics |
| Products | Platelets Pheresis |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected in an expired collection bag, was distributed. |
| Initiation date | May 10, 2002 |
| Termination date | Jan 13, 2005 |
| City | Stockton |
| Country | United States |
| FEI number | 2970116 |
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