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Daavlin Distributing Recalls
6 recalls on record · May 18, 2022 to July 22, 2026 · Medical Devices
Recalls by year
22
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 22, 2026Medical DevicesFDA
Daavlin Distributing Company recalls Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Hazard: 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).
July 22, 2026Medical DevicesFDA
Daavlin Distributing Company recalls Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Hazard: 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).
July 22, 2026Medical DevicesFDA
Daavlin Distributing Company recalls Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Hazard: 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).
June 10, 2026Medical DevicesFDA
Daavlin Distributing Company recalls Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psor
Hazard: Some of the Calibration/Output Certificates had the outputs reversed.
May 18, 2022Medical DevicesFDA
Daavlin Distributing Company recalls 4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. M4
Hazard: Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.
May 18, 2022Medical DevicesFDA
Daavlin Distributing Company recalls 1 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. Mode
Hazard: Software issue, resuming an interrupted treatment will result in swap of utilized calibration treatment distance 0" inches to "9. Resulting in over or under dosing.