Device recall
Z-2502-2018: VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961…
FDA device recall · Class II · Maquet SAS
Key facts
| Recall number (Z-number) | Z-2502-2018 |
|---|---|
| Recall event | 80452 |
| Product | VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF AIM STP; ARD568821911 VLT600SF AIM STP QL; ARD568821910 VLT600SF STP QL; ARD568811901 VLT600SF AIM STP Product Usage: The Maquet VOLISTA surgical lights are designed to illuminate… |
| Product code | FTD |
| Recalling firm | Maquet SAS |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2022 |
| 510(k) numbers | K130513 |
| FEI number | 3002465150 |
At a glance
- 1–9 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