# FDA recall Z-2571-2025

> **BigTree Sales Inc.** · Class II · device recall initiated 2025-08-29.

## Product

The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

## Reason for recall

The subject product emits unsafe level of UVC radiation (i.e., the product reaches the exposure limit for Risk Group 3 (high risk) in about 2.2 minutes). The product has a radiation safety defect, in that these radiation emissions are unnecessary to the accomplishment of the product s primary purpose of disinfecting objects and surfaces, and create a risk of skin and/or eye injuries to user and nearby persons.

## Distribution

U.S.A

## Key facts

- **Recall number:** Z-2571-2025
- **Recalling firm:** BigTree Sales Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-29
- **Report date:** 2025-09-24

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Arcadia, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2571-2025

## Citation

> AI Analytics. FDA recall Z-2571-2025. Retrieved 2026-08-03 from https://api.ai-analytics.org/recall/Z-2571-2025. Source: US FDA. Licensed CC0.

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