Drug recall
Cryoprecipitated, AHF
FDA recall event 34668 · Class II · Florida's Blood Centers, Inc.
Key facts
| Event ID | 34668 |
|---|---|
| Recall numbers | B-1237-6, B-1238-6 |
| Recalling firm | Florida's Blood Centers, Inc. |
| Product type | Biologics |
| Products | Cryoprecipitated, AHF, Recovered Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were collected from an unsuitable donor based on risk factors for variant Creutzfeldt-Jakob Disease 9vCJD), were distributed., Blood products, which were collected from an unsuitable donor based on risk factors for variant Creutzfeldt-Jakob Disease (vCJD), were distributed. |
| Initiation date | Apr 22, 2003 |
| Termination date | Jun 22, 2009 |
| City | Orlando |
| State | FL |
| Country | United States |
| FEI number | 1072425 |
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