# FDA recall Z-1292-2022

> **Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)** · Class II · device recall initiated 2022-04-21.

## Product

ProudP Everyday Uroflow Tracker  Software Version 1.x.x    Software Version 1.2.0 or earlier

## Reason for recall

Due to interference with the Live Listen feature of hearing aid or AirPods, the user's iPhone may perform automatic processing of the urination sound signal, resulting in lower urination volume and velocity values than expected.

## Distribution

Worldwide distribution - US Nationwide. The software app is distributed via the Apple App Store.

## Key facts

- **Recall number:** Z-1292-2022
- **Recalling firm:** Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-21
- **Report date:** 2022-07-06
- **Termination date:** 2023-09-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Seoul, Korea (the Republic of)

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1292-2022

## Citation

> AI Analytics. FDA recall Z-1292-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1292-2022. Source: US FDA. Licensed CC0.

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