{
  "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": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82068",
      "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": "The products were distributed to the following US states:  AL, CA, IL, MD, PA, TN, TX, UT, and WI.    The products were distributed to the following foreign countries:  Austria, Ecuador, Germany, Italy, Portugal, Romania, Saudi Arabia, and Spain.",
      "recall_number": "Z-1012-2019",
      "product_description": "Flexima Duodenal Bend Biliary Stent with Delivery System, 7F (2.3mm) x10cm, Material Number M00539220",
      "product_quantity": "75 units",
      "reason_for_recall": "The sterile barrier may contain packaging seal  defects.",
      "recall_initiation_date": "20181226",
      "center_classification_date": "20190314",
      "termination_date": "20200417",
      "report_date": "20190320",
      "code_info": "Lot 22960202"
    }
  ]
}