{
  "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": "86880",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "300 Boston Scientific Way",
      "address_2": "N/A",
      "postal_code": "01752-1291",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US nationwide and Japan.",
      "recall_number": "Z-0758-2021",
      "product_description": "Contour VL Variable Length Ureteral Stent Set, UPN M006180155090, M006180156090, M006180156180, M006180156190",
      "product_quantity": "458 units",
      "reason_for_recall": "Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.",
      "recall_initiation_date": "20201116",
      "center_classification_date": "20201230",
      "report_date": "20210106",
      "code_info": "GTIN 08714729423768: Lots 25928323, 25928324.     GTIN 08714729423829: Lots   25928325, 25928326, 25933063,  25933064, 25933065.     GTIN 08714729772743: Lot 25965814.     GTIN 08714729765837: Lot 25966020."
    }
  ]
}