{
  "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": [
    {
      "country": "United States",
      "city": "Gainesville",
      "address_1": "2320 NW 66th Ct",
      "reason_for_recall": "The Equinoxe Reverse Drill Bit Kits may contain two 2mm diameter drill bits instead of one 2mm diameter drill bit and one 3.2mm diameter drill bit as intended.",
      "address_2": "",
      "product_quantity": "2 units",
      "code_info": "Serial Numbers:  5214432, 5214445",
      "center_classification_date": "20181002",
      "distribution_pattern": "In the countries of Australia and France",
      "state": "FL",
      "product_description": "Equinoxe Reverse Drill Bit Kit, Catalog Number 321-20-00    Product Usage:  Shoulder surgery",
      "report_date": "20181010",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Exactech, Inc.",
      "recall_number": "Z-0012-2019",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "80996",
      "more_code_info": "",
      "recall_initiation_date": "20180821",
      "postal_code": "32653-1630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}