---
title: "AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH10... — FDA record Z-0403-2024 | Is It on Recall"
description: "Affected lots of product may experience technical distortions to a greater extent than expected."
url: https://isitonrecall.com/recall/fda-device-z-0403-2024-audx-pro-mobile-medical-devices-for-hearing-examinations-model-number-soh100098-part-number-100098-a/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP — FDA record Z-0403-2024

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 Sep 26, 2023. 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**: AuDX PRO, mobile medical devices for hearing examinations, Model Number SOH100098, Part Number 100098-AUP
- **Reason**: Affected lots of product may experience technical distortions to a greater extent than expected.
- **Classification**: Class II
- **Recalling firm**: PATH
- **Quantity**: 23 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0403-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0403-2024%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 | UDI-DI: 04260223143298; Serial Numbers: 260446-260468 |

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

## Distribution

US States: FL, MO, OH, WI

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

- [Florida](https://isitonrecall.com/state/florida/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Wisconsin](https://isitonrecall.com/state/wisconsin/)

## Dates in the source

- **Report date**: Dec 6, 2023
- **Recall initiation date**: Sep 26, 2023
- **Center classification date**: Nov 24, 2023

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-0403-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [PATH records](https://isitonrecall.com/brand/path/)