Dain Technology recalls ProudP Uroflow Tracker software versions 1.2.0 or earlier due to potential interference with hearing aids and AirPods, causing inaccurate urination measurements on iPhone.
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.
Dain Technology recalls ProudP Everyday Uroflow Tracker software versions 1.2.0 or earlier because they can interfere with hearing aids and AirPods, causing iPhone to misread urination flow rates. This means users might get inaccurate measurements of how much urine they produce.
The software can interfere with hearing aids and AirPods, causing iPhone to automatically process urination sounds. This leads to lower urination volume and velocity values than what's actually happening, meaning users might get inaccurate flow measurements.
Users of ProudP Uroflow Tracker software versions 1.2.0 or earlier who have hearing aids or AirPods. Those with hearing aids are most at risk of inaccurate measurements.
Check if you have ProudP Uroflow Tracker software version 1.2.0 or earlier. The UDI code is (01)00860006184902(10)v1.x.x for affected versions.
Update to ProudP software version 1.3.0 or later to fix the interference issue.
The software can interfere with hearing aids and AirPods, causing iPhone to misread urination flow rates.
Check if you have ProudP Uroflow Tracker software version 1.2.0 or earlier. The UDI code is (01)00860006184902(10)v1.x.x for affected versions.
Update to ProudP software version 1.3.0 or later to fix the interference issue.
We’ve drafted a message you can send Dain Technology to request your refund or repair — edit it as you like.
Subject: Recall Z-1292-2022 — Dain Technology Dain Technology Hello, I own a Dain Technology that is covered by recall Z-1292-2022 from Dain Technology. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
