Device recall
Z-1844-2016: EZ Slide Battery/line powered hydraulic table with removable leg section and 21…
FDA device recall · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Recall number (Z-number) | Z-1844-2016 |
|---|---|
| Recall event | 74128 |
| Product | EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide Operating Table General Purpose Surgical Table |
| Product code | GDC |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 20, 2017 |
| 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