Drug recall
Cryoprecipitate AHF
FDA recall event 28159 · Class III · Blood Systems Inc
Key facts
| Event ID | 28159 |
|---|---|
| Recall numbers | B-0872-4 |
| Recalling firm | Blood Systems Inc |
| Product type | Biologics |
| Products | Cryoprecipitate AHF |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, was prepared from plasma that was not frozen within 8 hours of phlebotomy, was distributed. |
| Initiation date | Jan 25, 2002 |
| Termination date | Mar 8, 2004 |
| City | Reno |
| Country | United States |
| FEI number | 2971465 |
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