Device recall
Z-2120-2014: GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser…
FDA device recall · Class II · Nidek Inc
Key facts
| Recall number (Z-number) | Z-2120-2014 |
|---|---|
| Recall event | 68302 |
| Product | GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser Photocoagulator Model GYC -1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty. |
| Product code | GEX |
| Recalling firm | Nidek Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 16, 2014 |
| 510(k) numbers | K032085 |
| FEI number | 2936921 |
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