Drug recall
Cryoprecipitated AHF, Pooled
FDA recall event 70391 · Class III · Blood Systems, Inc.
Key facts
| Event ID | 70391 |
|---|---|
| Recall numbers | B-0393-15 |
| Recalling firm | Blood Systems, Inc. |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Pooled |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, in which component preparation/component not prepared in accordance with specifications, was distributed. |
| Initiation date | Dec 16, 2014 |
| Report date | Mar 4, 2015 |
| Termination date | Feb 23, 2015 |
| City | Las Vegas |
| State | NV |
| Country | United States |
| FEI number | 2971457 |
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: