Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 26464 · Class III · WE & Lela I Stewart Blood Center, Inc
Key facts
| Event ID | 26464 |
|---|---|
| Recall numbers | B-1403-3 |
| Recalling firm | WE & Lela I Stewart Blood Center, Inc |
| Product type | Biologics |
| Products | Platelets Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, that was labeled leukoreduced but was not tested for white blood cell count within the time frames required in the firm's standard operating procedures, was distributed. |
| Initiation date | Aug 23, 2001 |
| City | Tyler |
| Country | United States |
| FEI number | 1672331 |
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