FDA Device recall Z-1292-2022
ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
- FDA Device
- Class II
- terminated
- Published 2022-07-06
On 2022-07-06 the FDA classified a Class II recall of ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier by Dain Technology Subsidiary Of Soundable Health, citing 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 ur….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1292-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-04-21 |
| Published | 2022-07-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Dain Technology Subsidiary Of Soundable Health |
| Distribution | US |
Product
ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
Reason
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.
Identifiers
| code_info | prouP Version - 1.2.0 UDI Code: (01)00860006184902(10)v1.x.x |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1292-2022%22
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