{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Espoo",
      "state": "N/A",
      "country": "Finland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98918",
      "recalling_firm": "SURGIFY MEDICAL OY",
      "address_1": "Otakaari 5 I",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.",
      "recall_number": "Z-2563-2026",
      "product_description": "Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)",
      "product_quantity": "0",
      "reason_for_recall": "Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).",
      "recall_initiation_date": "20260430",
      "center_classification_date": "20260624",
      "report_date": "20260701",
      "code_info": "UDI: 06429811532274; All lots until the IFU update has been implemented"
    }
  ]
}