Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 49169 · Class III · Community Blood Center Of Gtr KC
Key facts
| Event ID | 49169 |
|---|---|
| Recall numbers | B-0349-13 |
| Recalling firm | Community Blood Center Of Gtr KC |
| Product type | Biologics |
| Products | Platelets Pheresis Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which may have been exposed to unacceptable temperatures during storage, were distributed. |
| Initiation date | Jul 9, 2008 |
| Report date | Nov 21, 2012 |
| Termination date | Nov 14, 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: