Device recall
Z-1840-2021: Myriad-LX Light Source-for delivery of light to the surgical field to enhance…
FDA device recall · Class II · Nico Corp.
Key facts
| Recall number (Z-number) | Z-1840-2021 |
|---|---|
| Recall event | 87882 |
| Product | Myriad-LX Light Source-for delivery of light to the surgical field to enhance visualization of tissue during resection Part Number NN-7013 The Myriad-LX light source is a high-intensity 300W Xenon illuminator with a touch screen and digital dimming controls. The source is fitted with a proprietary… |
| Product code | GEI |
| Recalling firm | Nico Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2024 |
| 510(k) numbers | K191599 |
| FEI number | 3007456622 |
At a glance
- 1–9 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