Every recall we track for Daavlin Distributing Company — 6 in all — plus the complaints and injury reports the public filed about them.
Daavlin recalls Photera 600 phototherapy devices with incorrect UV sensor calibration that may deliver unsafe UV levels for skin treatment.
Daavlin recalls Photera 400 phototherapy devices with incorrect UV sensor calibration that may cause unsafe light exposure levels.
Daavlin recalls 32 Photera 600 3-D phototherapy devices with serial numbers starting with 6-09... due to incorrect UV sensor calibration that may lead to insufficient UV exposure for skin conditions.
Daavlin recalls Phothera 200 phototherapy devices with model numbers 210NDT4 and 210NCL4 where calibration certificates had outputs reversed. Affected units include specific serial numbers listed in the recall notice.
Daavlin recalls 4 Series CX phototherapy units with specific software versions due to risk of incorrect dosing from treatment interruptions. Affected units have ClearLink Control System software v3.03h or v3.04v.
Daavlin recalls 1 Series CX phototherapy units with specific software versions that may cause incorrect light therapy dosing if treatment is interrupted.
