{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65166",
      "recalling_firm": "Linvatec Corp. dba ConMed Linvatec",
      "address_1": "11311 Concept Blvd",
      "address_2": "N/A",
      "postal_code": "33773-4908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Distribution including the states of  FL, KY, LA, MI, NC, and NY.",
      "recall_number": "Z-1619-2013",
      "product_description": "GENESYS Cross FT Suture Anchor with Two #2 (5 metric) Hi-FI Registered Trade Mark Sutures Rx Only STERILE EO CONMED LINVATEC REF CFBC-4502.     Reattachment of soft tissue to bone in orthopedic surgical procedures",
      "product_quantity": "60 each of both units",
      "reason_for_recall": "Incorrect blue/white suture was used.",
      "recall_initiation_date": "20130306",
      "center_classification_date": "20130701",
      "termination_date": "20130722",
      "report_date": "20130710",
      "code_info": "Product Number CFBC-4502, Lot  #431437"
    }
  ]
}