{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Naples",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86021",
      "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": "International distribution in the countries of Denmark, United Kingdom, Sweden, Japan, Netherlands",
      "recall_number": "Z-2733-2020",
      "product_description": "Sterile Low Profile Screw, Titanium, 6.7 x 65mm  Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.",
      "product_quantity": "28 units",
      "reason_for_recall": "Screws provided in packaging are 5mm shorter than intended",
      "recall_initiation_date": "20200624",
      "center_classification_date": "20200729",
      "termination_date": "20210216",
      "report_date": "20200805",
      "code_info": "Batch Number: 10706233  UDI Number:00888867056411"
    }
  ]
}