{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Maple Grove",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "76002",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "2 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AZ, FL, MO, NJ, NY, OH, PA, and TX.",
      "recall_number": "Z-1781-2017",
      "product_description": "Boston Scientific Imager II Angiographic Catheter, M001316581 (5-pack outer package  UPN), M001316580, single unit, inner package UPN)",
      "product_quantity": "26 boxes of 5 (130 singles)",
      "reason_for_recall": "One lot of Imager II Angiographic Catheters is being recalled due to packaging mislabeling.  The product may be labeled as Imager II Contra 2 curve catheters, when in fact the package contains Contra curve catheters.",
      "recall_initiation_date": "20161213",
      "center_classification_date": "20170411",
      "termination_date": "20171122",
      "report_date": "20170419",
      "code_info": "Lot:  00116127, Expiration Date:  September 30, 2018",
      "more_code_info": ""
    }
  ]
}