FDAFDA · Food and drugs·Recall number Z-2743-2026
Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Published July 22, 2026 · Recall initiated: March 5, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the 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).
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Manufacturer
- Daavlin Distributing Company
- Distributor
- US Nationwide distribution.
- Lot
- Serial Numbers: 6-09033NB4CL, 6-09037NB4CL, 6-09031NB4CL, 6-09538NB4CL, 6-09038NB4CL, 6-09039NB4CL, 6-09040NB4CL, 6-09041NB4CL, 6-09035NB4CL, 6-09034NB4CL, 6-09030NB4CL, 6-09026NB4CL, 6-09023NB4CL, 6-09028NB4CL, 6-09025NB4CL, 6-09043NB4CL, 6-09029NB4CL, 6-09044NB4CL, 6-09022NB4CL, 6-09027NB4CL, 6-09036NB4CL, 6-09045NB4CL, 6-09024NB4CL, 6-07827NB4CL, 6-09539NB4CL, 6-09042NB4CL.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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