Reported Jul 22, 2026 · Ongoing

Photera 400, 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 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Lot codes and dates
  • Serial Numbers
    • 4-01440NB10CL
    • 2 4-01441NB10CL
Amount recalled
2 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, 7:01 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.