Drug recall
Cryoprecipitated AHF
FDA recall event 35710 · Class II · Bergen Comm Reg Blood Center
Key facts
| Event ID | 35710 |
|---|---|
| Recall numbers | B-1614-6 |
| Recalling firm | Bergen Comm Reg Blood Center |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which did not meet acceptable product specifications, were distributed. |
| Initiation date | Oct 27, 2004 |
| Termination date | Aug 14, 2006 |
| City | Paramus |
| Country | United States |
| FEI number | 2275064 |
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