Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 69351 · Class II · Blood Systems, Inc
Key facts
| Event ID | 69351 |
|---|---|
| Recall numbers | B-0072-15 |
| Recalling firm | Blood Systems, Inc |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, for which donor screening testing may not have been performed according to manufacturer's specifications, were distributed. |
| Initiation date | Aug 22, 2014 |
| Report date | Oct 29, 2014 |
| Termination date | Oct 22, 2014 |
| City | Fargo |
| State | ND |
| Country | United States |
| FEI number | 1771452 |
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: