{
  "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": "2026-04-01",
    "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": "86746",
      "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": "Nationwide  Foreign: Canada, Thailand, Taiwan, South Africa",
      "recall_number": "Z-0650-2021",
      "product_description": "Infinity ACL Tibial Elbow Guide-indicated for use in open and arthroscopic procedures for knee ligament reconstruction.  Catalog Number: KTE100",
      "product_quantity": "73 total: 23 units US;50 units OUS",
      "reason_for_recall": "Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially misaligned laterally which could affect the accuracy of the guide system",
      "recall_initiation_date": "20201112",
      "center_classification_date": "20201221",
      "termination_date": "20240405",
      "report_date": "20201230",
      "code_info": "Lot Codes:  201926AB  201942AF  201947AF  202007AF  202011 AF  202015AF  202018AF  202024AF"
    }
  ]
}