{
  "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-1189-2016",
      "product_description": "Universal Clamp¿ System (IFU reference: SNA027-N-90001).    Provides the stability required for solid bone fusion and helps reduce spinal deformities and fractures.",
      "product_quantity": "3484",
      "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"
    }
  ]
}