{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Domat/Ems",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99035",
      "recalling_firm": "Hamilton Medical AG",
      "address_1": "Parc Industrial Vial 10",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, IL, KY, MA, MI, \tND, NE, NE, NY, OH, PA, PR, SD, TX, VA, WA, WI, WV, WY and the country of Canada.",
      "recall_number": "Z-2625-2026",
      "product_description": "IntelliCuff, Portable automatic cuff pressure controller  REF: 951001",
      "product_quantity": "962 units",
      "reason_for_recall": "Due to reported complaints, the cuff device may alarm with a \"Cuff System Leakage\" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.",
      "recall_initiation_date": "20260522",
      "center_classification_date": "20260701",
      "report_date": "20260708",
      "code_info": "GTIN: 07630002800839/ Lot # range: 00001 -19732"
    }
  ]
}