Device recall
Z-0867-2011: Stryker Digital Capture Pro 2 device (240-050-800, CD version) and (240-050-810…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0867-2011 |
|---|---|
| Recall event | 54651 |
| Product | Stryker Digital Capture Pro 2 device (240-050-800, CD version) and (240-050-810, DVD version) designed for digital documentation of medical procedures. Manufactured by Stryker Endoscopy, San Jose, CA. |
| Product code | LMD |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 8, 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