Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 40101 · Class III · American National Red Cross (The) - North Central Region
Key facts
| Event ID | 40101 |
|---|---|
| Recall numbers | B-1436-08, B-1437-08 |
| Recalling firm | American National Red Cross (The) - North Central 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 product, collected under conditions where the sterility of the product may have been compromised, was distributed |
| Initiation date | May 19, 2005 |
| Termination date | May 30, 2008 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2173038 |
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