{
  "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-1740-2020",
      "product_description": "Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor     UPN: M006192132080",
      "product_quantity": "19 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 Numbers: 24749818, 24913418"
    }
  ]
}