{
  "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": "82691",
      "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": "Worldwide distribution to Australia, Belgium, Brazil, Chile, Colombia, Egypt, France, Germany, Great Britain, India, Indonesia, Iran, Italy, Lebanon, Malaysia, Mexico, Romania, Russia Fed., South Africa, South Korea, Spain, Taiwan, United Arab Emirates and Vietnam",
      "recall_number": "Z-1392-2019",
      "product_description": "AURIGA XL 4007 GENERAL SYSTEM   UPN: M0068FS4007G0    Product Usage:  The Auriga  XL 4007 Laser System and the Auriga  30 Laser System including a fiber optic delivery system is intended to be used in surgical procedures such as open, laparoscopic and endoscopic, to perform incision, excision, resection, ablation, vaporization, coagulation and hemostasis of soft tissue in medical specialties including: Urology, Urinary Lithotripsy, Gastroenterology, Arthroscopy, Discectomy, Pulmonary, Gynaecology, ENT, Dermatology, Plastic Surgery and General Surgery.",
      "product_quantity": "27 (OUS)",
      "reason_for_recall": "Certain Auriga consoles may exhibit faster than normal power degradation due to a potential issue in the mechanical cooling system that could lead to a low power error (1301) being displayed on the screen. The console is designed to stop emitting laser pulses and enters a stand-by mode after a low power error message.",
      "recall_initiation_date": "20190408",
      "center_classification_date": "20190522",
      "termination_date": "20230510",
      "report_date": "20190529",
      "code_info": "Serial Number:   21302771, 21302815, 21302786,  21302800, 21302843, 21302928,  21302842, 21302915, 21302900,  21302933, 21302783, 21302922,  21302934, 21302935, 21302942,  21302956, 21302957, 21302989,  21303002, 21303000, 21303001,  21303067, 21303004, 21303044,  21303042, 21302899, 21303091"
    }
  ]
}