Photera 400 Phototherapy Device
Daavlin recalls Photera 400 phototherapy device due to incorrect UV sensor gain causing inaccurate output.
Stop using the Photera 400 phototherapy device and contact Daavlin Distributing Company for instructions on inspection and recalibration.
Why it was recalled
Daavlin Distributing Company is recalling the Photera 400 phototherapy device because the calibrated output was not calculating correctly, with the UV sensor gain being applied incorrectly, potentially delivering incorrect UV doses.
Is mine affected?
This recall covers the products below. If you have any of them, yours is affected.
| Product | Recall # |
|---|---|
| Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders | Z-2744-2026 |
| Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders | Z-2742-2026 |
| Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders | Z-2743-2026 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Editorial summary by Recall Canary · summary updated 2026-08-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification