{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Seoul",
      "state": "",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90165",
      "recalling_firm": "Dain Technology, Inc. (Subsidiary of Soundable Health, Inc.)",
      "address_1": "Seocho-Daero, Seocho",
      "address_2": "# 413 398 Platinum Tower",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide. The software app is distributed via the Apple App Store.",
      "recall_number": "Z-1292-2022",
      "product_description": "ProudP Everyday Uroflow Tracker  Software Version 1.x.x    Software Version 1.2.0 or earlier",
      "product_quantity": "41 devices (out of 1,260 users)",
      "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.",
      "recall_initiation_date": "20220421",
      "center_classification_date": "20220627",
      "termination_date": "20230929",
      "report_date": "20220706",
      "code_info": "prouP Version - 1.2.0 UDI Code: (01)00860006184902(10)v1.x.x",
      "more_code_info": ""
    }
  ]
}