Device recall
Z-0578-2008: TENET Medical Engineering Wrist Stabilization Kit, Medium; REF (Part) #7692…
FDA device recall · Class II · Tenet Medical Engineering Inc
Key facts
| Recall number (Z-number) | Z-0578-2008 |
|---|---|
| Recall event | 46158 |
| Product | TENET Medical Engineering Wrist Stabilization Kit, Medium; REF (Part) #7692; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada T2Z 4M3. |
| Product code | JEB |
| Recalling firm | Tenet Medical Engineering Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2009 |
| FEI number | 3004750931 |
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