Drug recall
Cryoprecipitate, AHF
FDA recall event 31003 · Class II, Class III · American National Red Cross Great Lakes Region
Key facts
| Event ID | 31003 |
|---|---|
| Recall numbers | B-0679-7, B-0680-7, B-0681-7, B-0682-7, B-0683-7, B-0684-7, B-0685-7, B-0686-7, B-0687-7, B-0688-7, B-0689-7 |
| Recalling firm | American National Red Cross Great Lakes Region |
| Product type | Biologics |
| Products | Cryoprecipitate, AHF, Cryoprecipitate, Pooled, Fresh Frozen Plasma, Plasma Cryoprecipitated Reduced, Platelets. and 6 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed. |
| Initiation date | Mar 19, 2003 |
| Termination date | Feb 9, 2007 |
| City | Lansing |
| Country | United States |
| FEI number | 1873033 |
At a glance
- 10–99 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