Drug recall
Cryoprecipitated AHF
FDA recall event 27968 · Class III · Lifesource
Key facts
| Event ID | 27968 |
|---|---|
| Recall numbers | B-0657-4, B-0658-4 |
| Recalling firm | Lifesource |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Red Blood Cells |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, manufactured from Whole Blood units that were stored at an incorrect temperature, were distributed. |
| Initiation date | Sep 19, 2003 |
| Termination date | Apr 13, 2004 |
| City | Glenview |
| Country | United States |
| FEI number | 1472204 |
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