Daavlin Distributing Company: Light, Ultraviolet, Dermatological
Recall Summary Daavlin Distributing Company is recalling Photera 400 phototherapy devices and ultraviolet lamps used for treating skin disorders because the UV output calibration is not calculating correctly—the devices are delivering less ultraviolet radiation than intended due to a sensor error. The recall affects devices distributed nationwide across all U.S. states and Washington, D.C. This is classified as a Class II recall, which indicates a serious issue though not one likely to cause severe harm.
- Recalling firm
- Daavlin Distributing Company
- Product
- Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
- Reason
- Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-05
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9c4ebc1d-9642-4bb9-a160-6ccd27faf595