{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Utica",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77039",
      "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": "Letter",
      "distribution_pattern": "CA, IN, KS, MD, NY, OH, PA, TN, TX & WI",
      "recall_number": "Z-0253-2018",
      "product_description": "Nonabsorbable suture anchor system intended to reattach soft tissue to bone in orthopedic surgical procedures may be used in either arthroscopic or open surgical procedures.",
      "product_quantity": "56 units",
      "reason_for_recall": "Manufactured with the incorrect anchor outer body",
      "recall_initiation_date": "20170417",
      "center_classification_date": "20171214",
      "termination_date": "20210831",
      "report_date": "20171220",
      "code_info": "Lot Number 786351"
    }
  ]
}