Device recall
Z-1581-2016: reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage…
FDA device recall · Class II · LED Technologies, LLC
Key facts
| Recall number (Z-number) | Z-1581-2016 |
|---|---|
| Recall event | 73779 |
| Product | reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a device designed to deliver LED light spectrum in 880nm and 660nm directly into the body tissue to increase circulation and temporarily relieve pain associated with muscle… |
| Product code | ILY |
| Recalling firm | LED Technologies, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2016 |
| 510(k) numbers | K081570 |
| FEI number | 3006315288 |
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