Drug recall
Platelets, Pheresis Leukocytes Reduced
FDA recall event 33870 · Class III · American National Red Cross Indiana-Ohio Region
Key facts
| Event ID | 33870 |
|---|---|
| Recall numbers | B-0779-6, B-0780-6 |
| Recalling firm | American National Red Cross Indiana-Ohio Region |
| Product type | Biologics |
| Products | Platelets, Pheresis Leukocytes Reduced, Platelets Pheresis Leukocytes Reduced Irradiated |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, Blood products, possible contaminated with coagulase-negative staphylococcus, were distributed., Blood products, Blood products, possible contaminted with coagulase-negative staphylococcus, were distributed. |
| Initiation date | Aug 20, 2005 |
| Termination date | Mar 24, 2006 |
| City | Fort Wayne |
| Country | United States |
| FEI number | 1873031 |
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