FDAFDA recall Z-2742-2026 · Jul 22, 2026
Daavlin Distributing Company: Photera 400 recall
Recall found
Product
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Reason for recall
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
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- Serial Numbers: 4-01440NB10CL, 2 4-01441NB10CL.
- Quantity
- 2 units
- Distribution
- US Nationwide distribution.
- Recalling firm
- Daavlin Distributing Company, Bryan, OH
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-03-05
Source: openFDA enforcement record Z-2742-2026 · search recall number Z-2742-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.