{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plymouth",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89184",
      "recalling_firm": "Uromedica Inc.",
      "address_1": "1840 Berkshire Ln N",
      "address_2": "N/A",
      "postal_code": "55441-3723",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, CO, KS, MD, TX, and WI.",
      "recall_number": "Z-0458-2022",
      "product_description": "UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.",
      "product_quantity": "18 devices",
      "reason_for_recall": "The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure.",
      "recall_initiation_date": "20211122",
      "center_classification_date": "20220105",
      "termination_date": "20230811",
      "report_date": "20220112",
      "code_info": "Lot numbers UM00794 and UM00817, UDI 00180668000106"
    }
  ]
}