Drug recall
Cryoprecipitated AHF
FDA recall event 35451 · Class II · Walter L. Shepeard Community Blood Center, Inc.
Key facts
| Event ID | 35451 |
|---|---|
| Recall numbers | B-1620-6, B-1621-6, B-1622-6, B-1623-6 |
| Recalling firm | Walter L. Shepeard Community Blood Center, Inc. |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Platelets, Recovered Plasma, Red Blood Cells |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were collected from a donor who may be at aincreased risk for HIV-1 Group O infection, were distributed., Blood products, which were collected from a donor who may be at increased risk for HIV-1 Group O infection, were distributed. |
| Initiation date | Mar 13, 2003 |
| Termination date | Aug 15, 2006 |
| City | Augusta |
| Country | United States |
| FEI number | 1046616 |
At a glance
- 1–9 Products in this recall
- None 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