{
  "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": "2026-04-08",
    "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": "79667",
      "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": "US Nationwide Distribution",
      "recall_number": "Z-1641-2018",
      "product_description": "Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments, DRILL GUIDES:  a) REF 6975205, 5mm  b) REF 6975206, 6mm  c) REF 6975207, 7mm    Product Usage:  The PRESTIGE LP  reusable instruments are intended for the surgical implantation of the PRESTIGE LP  Cervical Disc. Medtronic reusable instruments must be sterilized prior to initial use and must be cleaned and sterilized prior to each re-use.",
      "product_quantity": "231 units",
      "reason_for_recall": "The firm received complaints of drill bits breaking during use with the Prestige LP(TM) Cervical Disc System.  Subsequent investigation demonstrated the interaction of the drill guide and the drill bit may lead to drill bit breakage.",
      "recall_initiation_date": "20180313",
      "center_classification_date": "20180504",
      "termination_date": "20201102",
      "report_date": "20180516",
      "code_info": "a) REF 6975205, 5mm; UDI 00643169752979  Lot Number ID17K018  b) REF 6975206, 6mm; UDI 00643169752962   Lot Number ID17J009  c) REF 6975207, 7mm; UDI 00643169752955  Lot Numbers:  ID17K007, ID17L035"
    }
  ]
}