{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Montreal",
      "state": "",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89619",
      "recalling_firm": "Orthosoft, Inc. dba Zimmer CAS",
      "address_1": "3300-75 Queen St",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution in the states of AR, NY, OH, TN, TX and the countries of Canada and the Netherlands.",
      "recall_number": "Z-0721-2022",
      "product_description": "NavitrackER Kit A: Knee, Model Number 20-8000-000-07,",
      "product_quantity": "14 units US; 132 units OUS",
      "reason_for_recall": "The product was released for distribution without passing sterilization results, which could potentially lead to insufficient sterility of the product. The highest severity risk is infection leading to surgical intervention.",
      "recall_initiation_date": "20220107",
      "center_classification_date": "20220303",
      "report_date": "20220309",
      "code_info": "Lot number 110221A1  UDI Number (01)00889024304222 (17)231103(10)110221A1",
      "more_code_info": ""
    }
  ]
}