Drug recall
Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
FDA recall event 99331 · Class II · Daavlin Distributing Company
Key facts
| Event ID | 99331 |
|---|---|
| Recall numbers | Z-2742-2026, Z-2743-2026, Z-2744-2026 |
| Recalling firm | Daavlin Distributing Company |
| Product type | Devices |
| Products | Photera 400, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders, Photera 600 3-D, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders, Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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). |
| Initiation date | Mar 5, 2026 |
| Report date | Jul 22, 2026 |
| City | Bryan |
| State | OH |
| Country | United States |
| FEI number | 1526255 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: