Class II

Medical Device Recall: Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Daavlin Distributing Company · March 5, 2026

Reason for Recall

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).

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

26 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2743-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Daavlin Distributing Company Medical Device Recall: Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders | SafeCheck