{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Solna",
      "state": "",
      "country": "Sweden",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99439",
      "recalling_firm": "Maquet Critical Care AB",
      "address_1": "Rontgenvagen 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, GA, MN, NY.",
      "recall_number": "Z-2963-2026",
      "product_description": "GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.",
      "product_quantity": "9 units",
      "reason_for_recall": "The module did not undergo electrical safety tests and functional tests during production.",
      "recall_initiation_date": "20260630",
      "center_classification_date": "20260814",
      "report_date": "20260826",
      "code_info": "DUI/DI 07325710000304, Serial/Lot Numbers:  21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.",
      "more_code_info": ""
    }
  ]
}