Device recall
Z-0566-2016: Valve XS Atrium Retractor FC429R 52154756 The Valve XS Atrium Lift Retractor is…
FDA device recall · Class II · Aesculap, Inc.
Key facts
| Recall number (Z-number) | Z-0566-2016 |
|---|---|
| Recall event | 72712 |
| Product | Valve XS Atrium Retractor FC429R 52154756 The Valve XS Atrium Lift Retractor is used in heart surgery. The retractor is used for the temporary dilation of the left atrium in mitral valve surgery and for assistance in tricuspid valve surgery. |
| Product code | GAD |
| Recalling firm | Aesculap, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2016 |
| FEI number | 2916714 |
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