Drug recall
Red Blood Cells (Apheresis) Leukocytes Reduced
FDA recall event 66941 · Class III · Blood Systems, Inc
Key facts
| Event ID | 66941 |
|---|---|
| Recall numbers | B-0244-14 |
| Recalling firm | Blood Systems, Inc |
| Product type | Biologics |
| Products | Red Blood Cells (Apheresis) Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which did not meet the minimum requirement for Red Blood Cell recovery following leukoreduction, was distributed. |
| Initiation date | Aug 13, 2013 |
| Report date | Jan 8, 2014 |
| Termination date | Dec 27, 2013 |
| City | Billings |
| State | MT |
| Country | United States |
| FEI number | 1771461 |
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: