Drug recall
Cryoprecipitated AHF
FDA recall event 26980 · Class III · ARC/New England Region
Key facts
| Event ID | 26980 |
|---|---|
| Recall numbers | B-1825-3 |
| Recalling firm | ARC/New England Region |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, lacking assurance of proper temperature storage during shipment, was distributed. |
| Initiation date | Jan 14, 2003 |
| 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