{
  "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": "76508",
      "recalling_firm": "Orthosoft, Inc. dba 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",
      "recall_number": "Z-1868-2017",
      "product_description": "SmartTools Knee System  Orthopedic Stereotaxic Instrument",
      "product_quantity": "84",
      "reason_for_recall": "There has been an increase in the number of complaints regarding bent or broken Drive Pins of the Validation Tool manufactured with drawing Revision M to P",
      "recall_initiation_date": "20170220",
      "center_classification_date": "20170419",
      "termination_date": "20170918",
      "report_date": "20170426",
      "code_info": "Lots:  130542A1  1405941  140146  140146-1  140147  140407A  140407A-1  140407B  140407-B-1  140860  140860-1  141035  150120  B150120  B150711"
    }
  ]
}