Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 65013 · Class II, Class III · Inland Northwest Blood Center
Key facts
| Event ID | 65013 |
|---|---|
| Recall numbers | B-1735-13, B-1736-13, B-1737-13 |
| Recalling firm | Inland Northwest Blood Center |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Cryoprecipitated AHF, Red Blood Cells Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed, Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed. |
| Initiation date | Mar 6, 2013 |
| Report date | Jun 5, 2013 |
| Termination date | May 24, 2013 |
| City | Spokane |
| State | WA |
| Country | United States |
| FEI number | 3071345 |
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: