Device recall
Z-0182-2009: Circlip component of the Stryker Flat Panel and Navigation Arm System. Stryker…
FDA device recall · Class II · Stryker Communications Corp
Key facts
| Recall number (Z-number) | Z-0182-2009 |
|---|---|
| Recall event | 49514 |
| Product | Circlip component of the Stryker Flat Panel and Navigation Arm System. Stryker Flat Panel and Navigation Arm System are intended for use as a ceiling-mounted device to support a medical grade flat panel monitor or camera in the patient area. The Circlip within the flat panel and navigation arms is… |
| Product code | FQO |
| Recalling firm | Stryker Communications Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 2, 2009 |
| FEI number | 3002975342 |
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