Drug recall
Cryoprecipitated AHF
FDA recall event 31110 · Class III · Mississippi Blood Services Inc
Key facts
| Event ID | 31110 |
|---|---|
| Recall numbers | B-0823-5, B-0824-5, B-0825-5, B-0826-5, B-0827-5, B-0828-5, B-0829-5, B-0830-5, B-0831-5 |
| Recalling firm | Mississippi Blood Services Inc |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Fresh Frozen Plasma, Plasma. Cryoprecipitated Reduced, Platelets, Platelets Pheresis, Leukocytes Reduced and 4 more |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, incorrectly tested for human immunodeficiency virus type 1 (HIV-1) antigen, were distributed. |
| Initiation date | Sep 30, 2003 |
| Termination date | Apr 29, 2005 |
| City | Jackson |
| Country | United States |
| FEI number | 1048744 |
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