{
  "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": "Marlborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77431",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "100 Boston Scientific Way",
      "address_2": "N/A",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MI, MO  Foreign:  Austria  France  Great Britain  Italy  Spain  Sweden",
      "recall_number": "Z-2673-2017",
      "product_description": "Boston Scientific Extractor Pro RX-S Retrieval Balloon Catheter  9-12mm Above  UPN: M00547300",
      "product_quantity": "39 units",
      "reason_for_recall": "Label on the affected devices incorrectly identifies the   injection location as \"above\" the balloon when it should be below the balloon and \"below\" the balloon when it should be above the balloon",
      "recall_initiation_date": "20170601",
      "center_classification_date": "20170703",
      "termination_date": "20180626",
      "report_date": "20170712",
      "code_info": "Lot Number: 19343203  Exp.: 6/30/2018"
    }
  ]
}