{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Marlborough",
      "address_1": "100 Boston Scientific Way",
      "reason_for_recall": "Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size",
      "address_2": "",
      "product_quantity": "38 units",
      "code_info": "Lot Number: 16231174",
      "center_classification_date": "20140110",
      "distribution_pattern": "Worldwide Distribution - USA (Nationwide Distribution and Puerto Rico) and Internationally.",
      "state": "MA",
      "product_description": "Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm Injects Above  UPN: M00547110",
      "report_date": "20140122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Boston Scientific Corporation",
      "recall_number": "Z-0711-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67139",
      "termination_date": "20140819",
      "more_code_info": "",
      "recall_initiation_date": "20131218",
      "postal_code": "01752-1234",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}