---
title: "The product is a handheld ultraviolet-C germicidal wand and contains a narrow... — FDA record Z-2571-2025 | Is It on Recall"
description: "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 pr"
url: https://isitonrecall.com/recall/fda-device-z-2571-2025-the-product-is-a-handheld-ultraviolet-c-germicidal-wand-and-contains-a-narrow-diameter-tubular-lamps/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# The product is a handheld ultraviolet-C germicidal wand and contains a narrow-diameter, tubular lamps with a peak emi... — FDA record Z-2571-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 29, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class II
- **Recalling firm**: BigTree Sales Inc.
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2571-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2571-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | SKU BT-GERMWAND-LRG-WHT and Testing: September 8-10, 2020 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.A

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 24, 2025
- **Recall initiation date**: Aug 29, 2025
- **Center classification date**: Sep 18, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2571-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [BigTree Sales Inc. records](https://isitonrecall.com/brand/bigtree-sales-inc/)