---
title: "BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U — FDA record Z-2184-2025 | Is It on Recall"
description: "Laryngoscope handles may not illuminate as intended."
url: https://isitonrecall.com/recall/fda-device-z-2184-2025-britepro-solo-mini-with-pro-miller-blade-size-1-5-ref-040-02-0415u/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U — FDA record Z-2184-2025

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 Jul 11, 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**: BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U
- **Reason**: Laryngoscope handles may not illuminate as intended.
- **Classification**: Class I
- **Recalling firm**: Flexicare Medical (Dongguan) Ltd.
- **Quantity**: N/A
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2184-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2184-2025%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 | Lots: 2007xxxxx to 2012xxxxx (July-2020 to Dec-2020) |

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

## Distribution

US Nationwide distribution in the states of WA, SD, TX, VA, PA, OK, GA, MI, WY, NC, OH.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alaska](https://isitonrecall.com/state/alaska/)
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- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
- [South Carolina](https://isitonrecall.com/state/south-carolina/)
- [South Dakota](https://isitonrecall.com/state/south-dakota/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [West Virginia](https://isitonrecall.com/state/west-virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Aug 13, 2025
- **Recall initiation date**: Jul 11, 2025
- **Center classification date**: Aug 1, 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-2184-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Flexicare Medical (Dongguan) Ltd. records](https://isitonrecall.com/brand/flexicare-medical-dongguan-ltd/)
