Drug recall
Human Tissue for Transplantation, Femoral Vein
FDA recall event 27665 · Class II · Cryolife Inc
Key facts
| Event ID | 27665 |
|---|---|
| Recall numbers | B-0388-4 |
| Recalling firm | Cryolife Inc |
| Product type | Biologics |
| Products | Human Tissue for Transplantation, Femoral Vein |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human tissue for transplantation, associated with tissue that was found to test positive for microorganisms at a different facility, was distributed. |
| Initiation date | Nov 4, 2003 |
| Termination date | Dec 15, 2003 |
| City | Kennesaw |
| Country | United States |
| FEI number | 3001451326 |
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