Device recall
Z-2295-2026: Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin…
FDA device recall · Class II · Daavlin Distributing Company
Key facts
| Recall number (Z-number) | Z-2295-2026 |
|---|---|
| Recall event | 98817 |
| Product | Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4 |
| Product code | FTC |
| Recalling firm | Daavlin Distributing Company |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K220840 |
| 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