{
  "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": "2026-09-30",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Versailles",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99641",
      "recalling_firm": "Midmark Corporation",
      "address_1": "60 Vista Dr",
      "address_2": "",
      "postal_code": "45380-9488",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-3217-2026",
      "product_description": "Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0320 with Kit Number: 4-000-0622",
      "product_quantity": "1 units",
      "reason_for_recall": "A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.",
      "recall_initiation_date": "20260821",
      "center_classification_date": "20260918",
      "report_date": "20260930",
      "code_info": "Model No: 1-200-0320; UDI-DI: 00841709105791; Kit No: 4-000-0622; UDI-DI: 00841709105876;  Kit Serial Number: V2900924; Zone Serial Number: V2899738",
      "more_code_info": ""
    }
  ]
}