{
  "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": "88684",
      "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": "Distribution in US: CA, MN, MO, NC, NV, NY, OH, OK, OR, PA, SC, SD, WA, WV",
      "recall_number": "Z-0085-2022",
      "product_description": "Endoskeleton\" TAS Interbody System with Titan nanoLOCK\" Surface Technology, Nanolock 12 Dg Interbody, Large, 12mm",
      "product_quantity": "10 units",
      "reason_for_recall": "Engraving on implants may not match what is listed on the pouch labels.",
      "recall_initiation_date": "20210902",
      "center_classification_date": "20211012",
      "termination_date": "20231005",
      "report_date": "20211020",
      "code_info": "Product Number 2312-0212-N, Lot A200323  GTIN 00191375014171"
    }
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}