Device recall
Z-2208-2014: Medical Positioning Rapid Response HUT table, Powered Medical Examination table…
FDA device recall · Class II · Medical Positioning Inc
Key facts
| Recall number (Z-number) | Z-2208-2014 |
|---|---|
| Recall event | 68763 |
| Product | Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to conduct syncope examinations. |
| Product code | LGX |
| Recalling firm | Medical Positioning Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 3, 2017 |
| FEI number | 1000118382 |
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