Device recall
Z-0655-2016: Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display…
FDA device recall · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Recall number (Z-number) | Z-0655-2016 |
|---|---|
| Recall event | 72897 |
| Product | Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for display interfaces utilized in clinical applications for viewing purposes and to provide an articulating point of movement on the ceiling mounted radial arm suspension system of the Ergon 2 equipment pendant / booms |
| Product code | FQO |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 19, 2016 |
| FEI number | 1825014 |
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