Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 43366 · Class III · Blood Systems, Inc.
Key facts
| Event ID | 43366 |
|---|---|
| Recall numbers | B-0280-14, B-0281-14 |
| Recalling firm | Blood Systems, Inc. |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced, 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 | Nov 10, 2006 |
| Report date | Jan 8, 2014 |
| Termination date | Jan 2, 2014 |
| City | Scottsdale |
| State | AZ |
| Country | United States |
| FEI number | 2071464 |
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: