Device recall
Z-0172-05: CryoValve, Aortic Valve & Conduit SG
FDA device recall · Class II · Cryolife Inc
Key facts
| Recall number (Z-number) | Z-0172-05 |
|---|---|
| Recall event | 30218 |
| Product | CryoValve, Aortic Valve & Conduit SG |
| Product code | MIE |
| Recalling firm | Cryolife Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2010 |
| FEI number | 3001451326 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database