{
  "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": "2026-04-29",
    "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": "71849",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "1 Scimed Pl",
      "address_2": "N/A",
      "postal_code": "55311-1565",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US including AZ, MO, OH and Internationally to GERMANY and SPAIN.",
      "recall_number": "Z-2378-2015",
      "product_description": "AngioJet SOLENT Omni Thrombectomy Set: UPN 109681-004 & 109681-001, Catalog No 109681,  Sterilized.                                                  For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking apart and removing thrombus from A-V access conduits.",
      "product_quantity": "total of 9 units",
      "reason_for_recall": "AngioJet products were distributed with an incorrect use-by (expiry) date.  The correct date is Nov-2015, but the units are labeled with a use-by date of Dec-2015.",
      "recall_initiation_date": "20150731",
      "center_classification_date": "20150813",
      "termination_date": "20160205",
      "report_date": "20150819",
      "code_info": "162185  162318"
    }
  ]
}