{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73265",
      "recalling_firm": "Zimmer Spine, Inc.",
      "address_1": "7375 Bush Lake Rd",
      "address_2": "N/A",
      "postal_code": "55439-2027",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed US (nationwide) and in the countries of Australia and Germany.",
      "recall_number": "Z-1019-2016",
      "product_description": "Virage OCT Spinal Fixation System.  Intended to promote fusion of the  Occipital-Cervical-Thoracic spine (Occiput-T3).",
      "product_quantity": "15,753",
      "reason_for_recall": "Zimmer Biomet Spine is initiating a Medical Device Correction regarding the Virage OCT Spinal Fixation System by providing additional guidance in the Virage OCT Surgical Technique Manual.",
      "recall_initiation_date": "20160203",
      "center_classification_date": "20160226",
      "termination_date": "20161011",
      "report_date": "20160309",
      "code_info": "Surgical Technique Manual  L1637 Rev B (2014-06)"
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}