Drug recall
Cryoprecipitated AHF
FDA recall event 50437 · Class II · Blood Systems, Inc.
Key facts
| Event ID | 50437 |
|---|---|
| Recall numbers | B-0198-15, B-0199-15, B-0200-15, B-0201-15, B-0202-15 |
| Recalling firm | Blood Systems, Inc. |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Plasma Frozen, Plasma Frozen Cryoprecipitated Reduced, Red Blood Cells (Apheresis) Leukocytes Reduced, Red Blood Cells Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who was taking Avodart, were distributed. |
| Initiation date | Nov 11, 2008 |
| Report date | Dec 10, 2014 |
| Termination date | Dec 4, 2014 |
| City | Scottsdale |
| State | AZ |
| Country | United States |
| FEI number | 2071464 |
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 · Source date: