{
  "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": "Wonju",
      "state": "N/A",
      "country": "Korea (the Republic of)",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85685",
      "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 Nationwide distribution.",
      "recall_number": "Z-2441-2020",
      "product_description": "DIRECT SUPPLY Attendant VITAL SIGNS MONITOR, REF AVSM2 - Product Usage: It is vital sign monitor 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": "180 devices",
      "reason_for_recall": "Failures were found in the temperature measurement function while in the predict mode.",
      "recall_initiation_date": "20200515",
      "center_classification_date": "20200626",
      "termination_date": "20220916",
      "report_date": "20200708",
      "code_info": "Serial Numbers:  456802000001~456802000180"
    }
  ]
}