{
  "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": "Memphis",
      "address_1": "1800 Pyramid Pl",
      "reason_for_recall": "Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.",
      "address_2": "",
      "product_quantity": "2 units",
      "code_info": "UDI:  00643169363502, Lot Number EM17F015",
      "center_classification_date": "20180209",
      "distribution_pattern": "MN, NC",
      "state": "TN",
      "product_description": "Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only",
      "report_date": "20180221",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "recall_number": "Z-0566-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78839",
      "termination_date": "20180731",
      "more_code_info": "",
      "recall_initiation_date": "20171222",
      "postal_code": "38132-1703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}