Device recall
Z-2743-2026: Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
FDA device recall · Class II · Daavlin Distributing Company
Key facts
| Recall number (Z-number) | Z-2743-2026 |
|---|---|
| Recall event | 99331 |
| Product | Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders |
| Product code | FTC |
| Recalling firm | Daavlin Distributing Company |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K212510 |
| FEI number | 1526255 |
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