Device recall
Z-0906-2011: InfraVision IR Illuminator Console, model number 220-180-521, manufactured by…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0906-2011 |
|---|---|
| Recall event | 56871 |
| Product | InfraVision IR Illuminator Console, model number 220-180-521, manufactured by Stryker Endoscopy San Jose, for use with the Stryker InfraVision system. Intended use:Medical device for human use, during surgical procedures to transilluminate anatomical structures during surgical procedures with… |
| Product code | FGS |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 9, 2011 |
| 510(k) numbers | K945297 |
| FEI number | 2936485 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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