{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Therwil, Baselland",
      "state": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62589",
      "recalling_firm": "Sentec AG",
      "address_1": "Ringstrasse 39",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution -- Nationwide including the state of  Missouri,. and the countries of  Germany, Spain, France, Netherlands, Australia, Belgium, Thailand.",
      "recall_number": "Z-2199-2012",
      "product_description": "SenTec, V-Sign\"2 Sensors     The SenTec Digital Monitoring System (SMDS) is used for continuous and noninvasive real-time monitoring of ventilation (tcPCO2) and oxygenation (SpO2).",
      "product_quantity": "8",
      "reason_for_recall": "SenTec is recalling a number of  V-Sign\"2 Sensors due to a problem regarding configuration parameter writing during manufacturing.",
      "recall_initiation_date": "20120709",
      "center_classification_date": "20120813",
      "termination_date": "20121011",
      "report_date": "20120822",
      "code_info": "310701  311100  311239  310996  311920  311943  311958  312132",
      "more_code_info": ""
    }
  ]
}