Device recall
Z-0657-2013: (l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat…
FDA device recall · Class II · Stryker Communications, Inc.
Key facts
| Recall number (Z-number) | Z-0657-2013 |
|---|---|
| Recall event | 63355 |
| Product | (l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring Arm Circlip is part of the Stryker Spring Arm used in multiple configurations as a component of the (1)Visum Halogen Surgical Light, (2)Visum LED Surgical Light, and (3)Stryker Flat… |
| Product code | FSY |
| Recalling firm | Stryker Communications, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 22, 2013 |
| FEI number | 3002975342 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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