Device recall
Z-1835-2014: The Claymount Harmony is a grid cabinet designed to accept a digital x-ray…
FDA device recall · Class II · Claymount Assembli
Key facts
| Recall number (Z-number) | Z-1835-2014 |
|---|---|
| Recall event | 67713 |
| Product | The Claymount Harmony is a grid cabinet designed to accept a digital x-ray imaging receptor and stationary grid. It contains signaling electronics to indicate the presence of the grid and detector as well as detector orientation. It may be mounted to a wall stand or incorporated in a radiographic… |
| Product code | IXY |
| Recalling firm | Claymount Assembli |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2018 |
| FEI number | 3006383214 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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