{
  "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": "Terminated",
      "city": "North Ryde, New South Wales",
      "state": "N/A",
      "country": "Australia",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87393",
      "recalling_firm": "Sirtex Medical Limited",
      "address_1": "Centrecourt Business Park,",
      "address_2": "Unit D4, 25-27, Paul Street North",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1275-2021",
      "product_description": "SIROS D-Vial Prep Set, Product Code SIR-10200 - Product Usage: intended for single use.",
      "product_quantity": "3310",
      "reason_for_recall": "There is a potential presence of particulate matter in the D-Vial.",
      "recall_initiation_date": "20210222",
      "center_classification_date": "20210318",
      "termination_date": "20230417",
      "report_date": "20210324",
      "code_info": "Lot Numbers: 1031234, 1031225, 1031227, 1031229"
    }
  ]
}