{
  "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": "2026-07-08",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Solna",
      "state": "",
      "country": "Sweden",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97032",
      "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 and Puerto Rico. No international distribution.",
      "recall_number": "Z-2015-2025",
      "product_description": "Servo-u MR Ventilator System. Model Number: 6888800.",
      "product_quantity": "129 units",
      "reason_for_recall": "Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.",
      "recall_initiation_date": "20250530",
      "center_classification_date": "20250627",
      "report_date": "20250709",
      "code_info": "Model Number: 6888800. UDI-DI: 07325710010518. All software versions.",
      "more_code_info": ""
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}