Drug recall
Cryoprecipitated AHF
FDA recall event 37906 · Class II · American National Red Cross (The)
Key facts
| Event ID | 37906 |
|---|---|
| Recall numbers | B-1391-07, B-1392-07, B-1393-07, B-1394-07, B-1395-07 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Fresh Frozen Plasma, Plasma Frozen Cryoprecipitate Reduced, Platelets, Platelets Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were manufactured from a whole blood unit in which an associated blood component contained clots, were distributed. |
| Initiation date | Apr 2, 2003 |
| Termination date | Aug 6, 2007 |
| City | Madison |
| State | WI |
| Country | United States |
| FEI number | 2173028 |
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