{
  "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": "Utica",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99498",
      "recalling_firm": "ConMed Corporation",
      "address_1": "525 French Rd",
      "address_2": "N/A",
      "postal_code": "13502-5945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of TX.",
      "recall_number": "Z-3018-2026",
      "product_description": "CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable  Driver  REF# CFBC-5502B  5.5mm GENESYs CrossFT Suture Anchor with  two, #2 (5 metric) Hi-Fi Sutures  Sterile",
      "product_quantity": "2 units",
      "reason_for_recall": "Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.",
      "recall_initiation_date": "20260714",
      "center_classification_date": "20260826",
      "report_date": "20260902",
      "code_info": "UDI:10845854042472, Lot number 1513167"
    }
  ]
}