Device recall
Z-1730-2014: Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area…
FDA device recall · Class II · Maquet Medical Systems USA
Key facts
| Recall number (Z-number) | Z-1730-2014 |
|---|---|
| Recall event | 68142 |
| Product | Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient. |
| Product code | FSY |
| Recalling firm | Maquet Medical Systems USA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2016 |
| FEI number | 3008355164 |
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