{
  "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": "Nashua",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80527",
      "recalling_firm": "Vascular Technology, Inc.",
      "address_1": "12 Murphy Drive",
      "address_2": "N/A",
      "postal_code": "03062-1903",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to state of: CA.",
      "recall_number": "Z-3026-2018",
      "product_description": "VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel  Ref. Number: 108910      Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.",
      "product_quantity": "10 units",
      "reason_for_recall": "Device maybe mislabeled as a 20 MHz Doppler transceiver instead of an 8 MHz Doppler transceiver",
      "recall_initiation_date": "20180619",
      "center_classification_date": "20180912",
      "termination_date": "20200130",
      "report_date": "20180919",
      "code_info": "Serial Numbers: 14329-001, 14329-002, 14329-003, 14329-004, 14329-005, 14329-006, 14329-007, 14329-008, 14329-009, and 14329-010."
    }
  ]
}