{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Gainesville",
      "address_1": "2320 NW 66th Ct",
      "reason_for_recall": "Potentially mislabeled.",
      "address_2": "",
      "product_quantity": "30",
      "code_info": "Catalog #: 314-13-03  Serial Range: 5013020 - 5013049",
      "center_classification_date": "20180126",
      "distribution_pattern": "Worldwide distribution in the states of OH, WI, AZ, GA, VA, CA, OK, MN, TN, ME, CO, SC, FL, AL, and Puerto Rico  and country of Switzerland",
      "state": "FL",
      "product_description": "Equinoxe Cage, Glenoid, Alpha, Medium    Product Usage:  The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the preferred method of treatment.",
      "report_date": "20180207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Exactech, Inc.",
      "recall_number": "Z-0415-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78903",
      "termination_date": "20190806",
      "more_code_info": "",
      "recall_initiation_date": "20170831",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}