{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Memphis",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87626",
      "recalling_firm": "Medtronic Sofamor Danek USA, Inc",
      "address_1": "4340 Swinnea Rd",
      "address_2": "N/A",
      "postal_code": "38118-6603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1440-2021",
      "product_description": "Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Large, 8 mm, Product Number 5146-1608-N - Product Usage: indicated to be used with supplemental fixation cleared by the FDA for use in the cervical spine and autograft bone, allograft bone comprised of cancellous and/or corticocancellous bone, demineralized allograft with bone marrow aspirate, or a combination thereof.",
      "product_quantity": "11 devices",
      "reason_for_recall": "The shelf box identifies a small device actually contains a large device, and the shelf box identifying a large device actually contains a small device.",
      "recall_initiation_date": "20210317",
      "center_classification_date": "20210420",
      "termination_date": "20230503",
      "report_date": "20210428",
      "code_info": "GTIN 00191375013167, Lot Number TM0126572",
      "more_code_info": ""
    }
  ]
}