{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Utica",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87578",
      "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": "International distribution in the countries of Canada, Italy.",
      "recall_number": "Z-1499-2021",
      "product_description": "KIT_INFINITY_BASE Custom Procedural Kit - Italy, containing Infinity ACL Tibial Elbow and Tip Guides product line, KTE100 and KTT100.    For use in open and arthroscopic procedures for knee ligament reconstruction    The procedural kits have no kit specific labeling.  Each product within the kits has its own product specific labeling.",
      "product_quantity": "3 units",
      "reason_for_recall": "Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system and could cause a delay in procedure and may require another device or alternate surgical method to be used",
      "recall_initiation_date": "20210326",
      "center_classification_date": "20210427",
      "termination_date": "20240405",
      "report_date": "20210505",
      "code_info": "Serial Numbers: 1, 2, 3",
      "more_code_info": ""
    }
  ]
}