Daavlin Distributing Company recalls Photera 600
- Recalling company
- Daavlin Distributing Company
- Product
- Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
- Reason
- 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).
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Mar 5, 2026
- Reported
- Jul 22, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 26 units
- Lot / codes
- 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.
- Company location
- Bryan, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2743-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2743-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.