Drug recall
Red Blood Cells Leukocytes Reduced
FDA recall event 40477 · Class III · Community Blood Center of Greater Kansas City
Key facts
| Event ID | 40477 |
|---|---|
| Recall numbers | B-2048-12 |
| Recalling firm | Community Blood Center of Greater Kansas City |
| Product type | Biologics |
| Products | Red Blood Cells Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which may have been exposed to unacceptable storage temperatures, were distributed. |
| Initiation date | Jul 28, 2005 |
| Report date | Jul 25, 2012 |
| Termination date | Jul 19, 2012 |
| City | Kansas City |
| State | MO |
| Country | United States |
| FEI number | 1972933 |
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 · Source date: