Drug recall
Cryoprecipitated AHF
FDA recall event 32349 · Class II, Class III · Blood Systems, Inc dba United Blood Services
Key facts
| Event ID | 32349 |
|---|---|
| Recall numbers | B-1727-5, B-1728-5, B-1729-5, B-1730-5, B-1731-5, B-1732-5, B-1733-5, B-1734-5, B-1735-5, B-1736-5 |
| Recalling firm | Blood Systems, Inc dba United Blood Services |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Plasma, Plasma, Cryoprecipitate Reduced, Platelets Pheresis, Leukocytes Reduced, Platelets Pheresis, Leukocytes Reduced Irradiated and 5 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from donors whose health history screenings were inadequately performed, were distributed. |
| Initiation date | Dec 3, 2004 |
| Termination date | Jul 27, 2005 |
| City | Scottsdale |
| Country | United States |
| FEI number | 2071464 |
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