Drug recall
Recovered Plasma
FDA recall event 32720 · Class II · ARC Blood Services, New England Region
Key facts
| Event ID | 32720 |
|---|---|
| Recall numbers | B-1935-5, B-1936-5 |
| Recalling firm | ARC Blood Services, New England Region |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor whose medical history interview did not have documentation to an answer to a medical history question related to Creutzfeldt-Jakob disease (CJD), were… |
| Initiation date | May 6, 2005 |
| Termination date | Aug 29, 2005 |
| City | Dedham |
| 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