Device recall
Z-1943-2021: inLight Medical LED Pads used with Polychromatic light technology system
FDA device recall · Class III · Inlightened Partners LLC
Key facts
| Recall number (Z-number) | Z-1943-2021 |
|---|---|
| Recall event | 85106 |
| Product | inLight Medical LED Pads used with Polychromatic light technology system |
| Product code | ILY |
| Recalling firm | Inlightened Partners LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 25, 2021 |
| 510(k) numbers | K153389 |
| FEI number | 3010709091 |
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