{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wonju",
      "state": "N/A",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88166",
      "recalling_firm": "Mediana Co., Ltd.",
      "address_1": "132 Donghwagongdan-Ro",
      "address_2": "Munmag-Eup",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Distribution to: Wisconsin only",
      "recall_number": "Z-2096-2021",
      "product_description": "AVSM3 SNF, Vital Signs Monitor    The monitor is intended to be used to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and hospital-type facilities.",
      "product_quantity": "618",
      "reason_for_recall": "In some cases the equipment fails to power up and/or key or button unresponsive or not working.",
      "recall_initiation_date": "20210517",
      "center_classification_date": "20210719",
      "termination_date": "20221104",
      "report_date": "20210728",
      "code_info": "Serial #(s) 460062000002 thru 460062000501 and 460062100033 thru 460062100150    UDI:(01)18800003460066",
      "more_code_info": ""
    }
  ]
}