Photera 400 — Class II medical device recall Z-2742-2026
Ongoing recall by Daavlin Distributing Company, reported 2026-07-22, distributed nationwide. Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to
| Recall number | Z-2742-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Daavlin Distributing Company, Bryan, OH, United States |
| Recall initiated | 2026-03-05 |
| Classified | 2026-07-15 |
| Reported by FDA | 2026-07-22 |
| Distributed | Nationwide (US) |
| Quantity | 2 units |
| Serial numbers | 4-01440NB10CL, 4-01441NB10CL |
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2742-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.