Drug recall
Cryoprecipitated AHF
FDA recall event 28519 · Class II · Lifeshare Inc
Key facts
| Event ID | 28519 |
|---|---|
| Recall numbers | B-1057-4 |
| Recalling firm | Lifeshare Inc |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, associated with a unit of Red Blood Cells that contained clots, was distributed. |
| Initiation date | Dec 29, 2003 |
| Termination date | May 1, 2004 |
| City | Elyria |
| Country | United States |
| FEI number | 1523639 |
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