Device recall
Z-1590-2010: An Imaging device for medical procedures, to provide surgeons or operating room…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-1590-2010 |
|---|---|
| Recall event | 54683 |
| Product | An Imaging device for medical procedures, to provide surgeons or operating room personnel the ability to capture still images and to record video during the surgical procedures in various file formats. Images can be transferred to external media. |
| Product code | LMB |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 17, 2011 |
| FEI number | 2936485 |
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