Device recall
Z-1506-2023: DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
FDA device recall · Class II · DermLite LLC
Key facts
| Recall number (Z-number) | Z-1506-2023 |
|---|---|
| Recall event | 91987 |
| Product | DERMLITE DL4W, REF: DL4W, Rx Only MD, CE |
| Product code | KYT |
| Recalling firm | DermLite LLC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3003452144 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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