Class II
Medical Device Recall: Photera 400, 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
2 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2742-2026
Status: ongoing
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