{
  "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": "Telford",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64447",
      "recalling_firm": "Draeger Medical, Inc.",
      "address_1": "3135 Quarry Rd",
      "address_2": "N/A",
      "postal_code": "18969-1042",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of CA, IL, and MA.",
      "recall_number": "Z-0939-2013",
      "product_description": "Draeger Infinity Acute Care System (IACS) Monitoring Solution. Catalog Number MS20783 (Infinity MCable-Dual Hemo)     Physiological patient monitoring system.",
      "product_quantity": "260",
      "reason_for_recall": "The displayed value for the invasive blood pressure measurement of the IACS was different than the actual patient values.  Liquid ingress in the cable connection may cause inaccurate measurements.  This can happen if the Dual Hemo MCable is used in a non-vertical position, a vertical position but upside down, or laying it on the floor or on the patient bed.",
      "recall_initiation_date": "20121213",
      "center_classification_date": "20130311",
      "termination_date": "20130520",
      "report_date": "20130320",
      "code_info": "Catalog Number MS20783 (Infinity MCable-Dual Hemo)",
      "more_code_info": ""
    }
  ]
}