Drug recall
Platelets, Leukocyte Reduced
FDA recall event 31389 · Class II · American Red Cross Blood Services Tennessee Valley Region
Key facts
| Event ID | 31389 |
|---|---|
| Recall numbers | B-0981-5 |
| Recalling firm | American Red Cross Blood Services Tennessee Valley Region |
| Product type | Biologics |
| Products | Platelets, Leukocyte Reduced |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, manufactured from an overweight unit of Whole Blood, was distributed. |
| Initiation date | Jun 14, 2004 |
| City | Nashville |
| Country | United States |
| FEI number | 1073006 |
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