Reported Jul 22, 2026 · Ongoing · Updated Sep 16, 2026
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
6-09033NB4CL6-09037NB4CL6-09031NB4CL6-09538NB4CL6-09038NB4CL6-09039NB4CL6-09040NB4CL6-09041NB4CL6-09035NB4CL6-09034NB4CL6-09030NB4CL6-09026NB4CL6-09023NB4CL6-09028NB4CL6-09025NB4CL6-09043NB4CL6-09029NB4CL6-09044NB4CL6-09022NB4CL6-09027NB4CL6-09036NB4CL6-09045NB4CL6-09024NB4CL6-07827NB4CL6-09539NB4CL6-09042NB4CL
- Serial Numbers
- 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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