{
  "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": "2026-04-29",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Winter Park",
      "address_1": "1300 Minnesota Ave",
      "reason_for_recall": "SpineNet was marketing this device to be used with SpineNet ACC device without FDA clearance or approval.",
      "address_2": "Suite 200",
      "product_quantity": "100 units",
      "code_info": "Lot # 22754F16 and #25854I17",
      "center_classification_date": "20130827",
      "distribution_pattern": "Distributed to one customer in Florida.",
      "state": "FL",
      "product_description": "SpineNet Bone Marrow Aspiration Needle Kit (which is the Ranfac Bone Marrow Aspiration Needle #74150-01M).    Use to aspirate bone morrow.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SpineNet",
      "recall_number": "Z-2107-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65914",
      "termination_date": "20131115",
      "more_code_info": "",
      "recall_initiation_date": "20130204",
      "postal_code": "32789-4800",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}