{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77352",
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "address_1": "1800 Pyramid Pl",
      "address_2": "N/A",
      "postal_code": "38132-1703",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "worldwide",
      "recall_number": "Z-2247-2017",
      "product_description": "KYPHON(R) Directional Bone Filler Device, Size: 3, REF F04C, Rx Only, STERILE R.",
      "product_quantity": "17657 units",
      "reason_for_recall": "The directional arrow at the proximal end of the instrument may not correctly align with the cut\u0010out opening on the distal end of the instrument. Using affected bone void filler may result in the injected cement being placed in a direction unintended by the surgeon.",
      "recall_initiation_date": "20170517",
      "center_classification_date": "20170603",
      "termination_date": "20190618",
      "report_date": "20170614",
      "code_info": "All Lots"
    }
  ]
}