Z-2742-2026 Class II Ongoing
FDA device recall Z-2742-2026 was initiated by Daavlin Distributing Company on March 5, 2026 and is designated Class II. 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). The recall status is ongoing. Affected quantity: 2 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 22, 2026
- Initiation Date
- March 5, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2 units
Product Description
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).
Distribution Pattern
US Nationwide distribution.
Code Information
Serial Numbers: 4-01440NB10CL, 2 4-01441NB10CL.