{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Bronshoj",
      "state": "N/A",
      "country": "Denmark",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85166",
      "recalling_firm": "Radiometer Medical ApS",
      "address_1": "Akandevej 21",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US: in the state of California",
      "recall_number": "Z-1836-2020",
      "product_description": "ABL800 FLEX model number 393-800 and 393-801, UDI:(01)05700693938004",
      "product_quantity": "2 units",
      "reason_for_recall": "Through internal investigation is has been determined that an incorrect component was used within the power supply. The incorrect component may cause a short circuit within the power supply resulting in a delay in treatment. The delay could result in a range of risk from  cyanosis and low blood pressure  to cardiac arrhythmias and severe impairment of cardiac function.",
      "recall_initiation_date": "20200306",
      "center_classification_date": "20200430",
      "report_date": "20200506",
      "code_info": "Serial Numbers: 902-754R2692N002 and 902-754R2692N001"
    }
  ]
}