{
  "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": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85227",
      "recalling_firm": "Boston Scientific",
      "address_1": "100 Boston Scientific Way",
      "address_2": "N/A",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign:  Europe, Middle East and Africa, the Americas (North America and South America,   Asia Pacific and  Japan",
      "recall_number": "Z-1735-2020",
      "product_description": "Percuflex Plus Ureteral Stent Set 7FX24CM with .035 Sensor  UPN: M006175272080 (edited 1/13/2021)",
      "product_quantity": "5 units",
      "reason_for_recall": "An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a  procedural delay due to the need to exchange the affected device",
      "recall_initiation_date": "20200309",
      "center_classification_date": "20200417",
      "report_date": "20200429",
      "code_info": "Lot Number: 24958079 (edited 1/13/2021)"
    }
  ]
}