# FDA recall Z-2743-2026

> **Daavlin Distributing Company** · Class II · device recall initiated 2026-03-05.

## Product

Photera 600, 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

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2743-2026
- **Recalling firm:** Daavlin Distributing Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-05
- **Report date:** 2026-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bryan, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2743-2026

## Citation

> MORVS. FDA recall Z-2743-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2743-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*