{
  "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": "Montreal",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71202",
      "recalling_firm": "Zimmer CAS",
      "address_1": "75 Queen St #3300",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including AL, AZ, CA,  CA,  CO,  FL, IN,  MI,  NJ,  NY,  OH, OR, PA, TX,  VA, and WI.",
      "recall_number": "Z-1701-2015",
      "product_description": "Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;",
      "product_quantity": "78 devices",
      "reason_for_recall": "Zimmer CAS has determined that the potential exists for the spikes on the iASSIST Tibial Alignment Guide to bend or break during insertion or extraction from the tibia during use.",
      "recall_initiation_date": "20150419",
      "center_classification_date": "20150602",
      "termination_date": "20160513",
      "report_date": "20150610",
      "code_info": "Item Number: 20-8011-013-00; Lot Numbers: 120265; 110623; 120659; 120794;120659-1; 130134; 120793; 130135"
    }
  ]
}