Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) 2022-07-06 Health serious FDA
Health · FDA · Recall #FDA-Z-1292-2022
ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or… Recall
Issued July 6, 2022 · Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)
In July 2022, Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) recalled the ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)
- Category
- Health
- Recall date
- July 6, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide. The software app is distributed via the Apple App Store.
- Recall number
- FDA-Z-1292-2022
- Made in
- Korea (the Republic of)
- Issuing agency
- FDA
In context
- Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.