Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 38910 · Class II, Class III · ARC Blood Services, New England Region
Key facts
| Event ID | 38910 |
|---|---|
| Recall numbers | B-0368-13, B-0369-13, B-0370-13, B-0371-13 |
| Recalling firm | ARC Blood Services, New England Region |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Plasma Frozen, Red Blood Cells Leukocytes Reduced Plasma Frozen, Red Blood Cells Rejuvenated Irradiated |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from donors, whose suitability to donate was not adequately determined, were distributed |
| Initiation date | Jun 13, 2007 |
| Report date | Dec 5, 2012 |
| Termination date | Nov 26, 2012 |
| City | Dedham |
| State | MA |
| Country | United States |
| FEI number | 1270026 |
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: