Reported Jul 22, 2026 · Ongoing

Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders

Daavlin Distributing Company

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Daavlin Distributing Company · 205 W Bement St · Bryan, OH · 43506-1264

Is this the product you have?

  • Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Lot codes and dates
  • 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
Amount recalled
26 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

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).

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.