{
  "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": "2026-08-20",
    "results": {
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      "product_res_number": "Z-0176-2007",
      "event_date_initiated": "2006-10-20",
      "event_date_posted": "2006-11-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-04-04",
      "res_event_number": "36701",
      "product_code": "LYS",
      "product_description": "Medtronic Sofamor Danek Bone fragmentor Ref Number/Model # 9150111",
      "code_info": "Lot numbers:  36197, 36200, 36198, 36199, 36196, 40591, 54685, 70942, 70605, 74679, 18150, 20271, 7935",
      "firm_fei_number": "1000477302",
      "recalling_firm": "Medtronic Sofamor Danek USA Inc",
      "address_1": "1800 Pyramid Place",
      "city": "Memphis",
      "state": "TN",
      "postal_code": "38132-1719",
      "additional_info_contact": "Jill Serbousek\n901-399-2912",
      "reason_for_recall": "Metal bone fragmentor was causing metal shavings to be released into the resultant fragmented tissue during use.",
      "root_cause_description": "Other",
      "action": "The firm notified its consignees of the problem and the recall by letter delivered via overnight mail on 10/20/2006.  The firm''s overseas distributors were also notified via electronic mail on 10/20/2006.  The notices requested the discontinuation of use and stated that sales representatives would be retrieving the devices from them.",
      "product_quantity": "255 units",
      "distribution_pattern": "Worldwide Distribution-USA and countries of The Netherlands, Hong Kong, and Japan.",
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