Daavlin recalls
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Daavlin and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-07-22FDA-DeviceClass IIDaavlin Photera 600 3-D phototherapy device recalled for incorrect UV calibration
The Photera 600 3-D ultraviolet phototherapy device used to treat skin disorders has a calibration error in how it calculates UV output. A sensor setting was incorrectly applied, causing the device to deliver lower UV intensity than intended. This affects 212 units distributed nationwide.
- 2026-07-22FDA-DeviceClass IIDaavlin Photera 600 phototherapy device recalled for incorrect UV output
The Photera 600 ultraviolet phototherapy device was found to have an error in how it calculates UV output. A sensor setting was incorrect, causing the device to deliver lower UV levels than intended. This affects 26 units with specific serial numbers distributed nationwide.
- 2026-07-22FDA-DeviceClass IIDaavlin Photera 400 phototherapy device recalled for incorrect UV calibration
The Photera 400 ultraviolet phototherapy device uses a sensor to measure and control UV output for treating skin disorders. A calibration error caused the sensor to report incorrect UV levels, which means patients may have received different doses than intended.
Get the week's recalls, including Daavlin
Free weekly digest — every federal recall affecting your household, Daavlin included when it comes up. Track Daavlin specifically with Always-on.