Drug recall
Cyroprecipitated AHF
FDA recall event 33542 · Class II · Belle Bonfils Memorial Blood Center
Key facts
| Event ID | 33542 |
|---|---|
| Recall numbers | B-0361-6 |
| Recalling firm | Belle Bonfils Memorial Blood Center |
| Product type | Biologics |
| Products | Cyroprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was not refrozen within one hour of preparation, was distributed. |
| Initiation date | Dec 7, 1999 |
| Termination date | Dec 8, 2005 |
| City | Denver |
| Country | United States |
| FEI number | 3000210247 |
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