Class II — Daavlin Distributing Company
| Recalling firm | THE DAAVLIN DISTRIBUTING CO. |
|---|---|
| Registered facility | THE DAAVLIN DISTRIBUTING CO. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| 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). |
| Product | Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders |
| Quantity | 26 units |
| Distribution | US Nationwide distribution. |
| Initiated | 2026-03-05 |
| Classified | 2026-07-15 |
| Recall number | Z-2743-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Daavlin Distributing Company (Z-2743-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99331/
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