Drug recall
Vascular Graft
FDA recall event 64210 · Class II · CryoLife, Inc.
Key facts
| Event ID | 64210 |
|---|---|
| Recall numbers | B-0768-13 |
| Recalling firm | CryoLife, Inc. |
| Product type | Biologics |
| Products | Vascular Graft |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human Tissues, recovered from a donor whose donor eligibility determination did not identify if the donor was free from risk factors for and clinical evidence of, infection due to relevant… |
| Initiation date | Dec 12, 2012 |
| Report date | Feb 6, 2013 |
| Termination date | Jan 31, 2013 |
| City | Kennesaw |
| State | GA |
| 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 · Source date: