Device recall
Z-1496-06: Skytron General Purpose Surgical Table; Model 6600, Dist. by Skytron, Grand…
FDA device recall · Class II · Skytron, Div. The KMW Group, Inc
Key facts
| Recall number (Z-number) | Z-1496-06 |
|---|---|
| Recall event | 35875 |
| Product | Skytron General Purpose Surgical Table; Model 6600, Dist. by Skytron, Grand Rapids, MI. |
| Product code | FQO |
| Recalling firm | Skytron, Div. The KMW Group, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2008 |
| 510(k) numbers | K950192 |
| FEI number | 1825014 |
At a glance
- 1–9 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