Drug recall
Platelets Pheresis, Leukocytes Reduced
FDA recall event 37455 · Class III · American National Red Cross
Key facts
| Event ID | 37455 |
|---|---|
| Recall numbers | B-1306-07, B-1307-07 |
| Recalling firm | American National Red Cross |
| 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, possibly collected without the entire amount of anticoagulant solution, were distributed., Platelet components were produced using equipment with malfunctioning AC alarms. |
| Initiation date | Oct 4, 2004 |
| Termination date | May 11, 2007 |
| City | Portland |
| Country | United States |
| FEI number | 3072996 |
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