{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73363",
      "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": "US (nationwide)-including the states of AL, AZ, AR, CA, CO, FL, GA, ID, IL, IN, IA, LA, ,MD, MA, MI, MN,MO, NV, NH, NY, NC, OH, OK,. PA, TN,TX, WA, and WI.",
      "recall_number": "Z-1190-2016",
      "product_description": "Instinct¿ Java¿ System (IFU reference: 046WAN0000T) .    Stabilizes one or more vertebral segments from the thoracic spine to the sacrum during the development of bone tissue.",
      "product_quantity": "2506",
      "reason_for_recall": "Zimmer Biomet is initiating a Medical Device Correction Notice to provide updated cleaning and disinfecting instructions for use of the Instinct¿ Java¿ System (IFU reference: 046WAN0000T) and Universal Clamp¿ System (IFU reference: SNA027-N-90001).",
      "recall_initiation_date": "20160212",
      "center_classification_date": "20160318",
      "termination_date": "20160811",
      "report_date": "20160330",
      "code_info": "All  lots"
    }
  ]
}