🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: April 21, 2022 Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.) Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    prouP Version - 1.2.0 UDI Code: (01)00860006184902(10)v1.x.x
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

prouP Version - 1.2.0 UDI Code: (01)00860006184902(10)v1.x.x

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1292-2022