Drug recall
Cryoprecipitated AHF
FDA recall event 30386 · Class II · American National Red Cross (The) - North Central Region
Key facts
| Event ID | 30386 |
|---|---|
| Recall numbers | B-0503-5, B-0504-5, B-0505-5, B-0506-5, B-0507-5, B-0508-5, B-0509-5, B-0510-5 |
| Recalling firm | American National Red Cross (The) - North Central Region |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Cryoprecipitated AHF, Pooled, Fresh Frozen Plasma, Granulocytes, Platelets Pheresis, Platelets and 3 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for antibody to human immunodeficiency virus type 1 (anti-HIV-1), but were collected from donors that previously tested repeatedly reactive for anti-HIV, were… |
| Initiation date | Jul 23, 1999 |
| Termination date | Feb 25, 2005 |
| City | Saint Paul |
| Country | United States |
| FEI number | 2173038 |
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