{
  "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,
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  "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-0757-2021",
      "product_description": "Contour VL Variable Length Ureteral Stent, UPN M0061801550, M0061801560, M0061801570",
      "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 08714729058410:   Lots   25578577, 25598812, 25609220,  25614542, 25614545, 25619687,  25641771, 25713852, 25753933,  25790349.     GTIN 08714729067986:   Lots   25640715, 25670518, 25686790,  25686791, 25686792, 25741763,  25741770, 25753937, 25790351,  25795704, 25802759, 25809481,  25822104.     GTIN 08714729068020:   Lots   25578740, 25583824."
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}