Device recall
Z-1774-2008: Hall Easy-Fit Prosthetic Heart Valve - Aortic A7700. The device uses a single…
FDA device recall · Class II · Medtronic Heart Valve Division
Key facts
| Recall number (Z-number) | Z-1774-2008 |
|---|---|
| Recall event | 47795 |
| Product | Hall Easy-Fit Prosthetic Heart Valve - Aortic A7700. The device uses a single pyrolytic carbon disc occluder pivoting within a titanium housing. The housing is machined into final configuration from a single piece of solid titanium and has no welds or introduced bends. It is an open-membered design… |
| Recalling firm | Medtronic Heart Valve Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2012 |
| PMA numbers | P790018, P790018S042 |
| FEI number | 2127690 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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