{
  "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": [
    {
      "status": "Terminated",
      "city": "Naples",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73579",
      "recalling_firm": "Arthrex, Inc.",
      "address_1": "1370 Creekside Blvd",
      "address_2": "N/A",
      "postal_code": "34108-1945",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed to the states of AR, AZ, CA, CO, FL, IL, IN, KS, KY, LA, MD, MO, NC, NJ, NV, NY, OH, PA, SD, TN, TX, and WI.",
      "recall_number": "Z-1360-2016",
      "product_description": "Arthrex Deltoid Ligament Reconstruction Implant System.    Intended as a fixation post, a distribution bridge or for distributing suture tension over areas of ligament or tendon repair utilizing titanium buttons.",
      "product_quantity": "117 devices",
      "reason_for_recall": "Potential for a component contained in the Implant System to be non-sterile.",
      "recall_initiation_date": "20160111",
      "center_classification_date": "20160408",
      "termination_date": "20190724",
      "report_date": "20160420",
      "code_info": "Unique Device Identifier: 00888867131446; Catalog No.: AR-8918CP; Batch No.: 10020303.",
      "more_code_info": ""
    }
  ]
}