{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Nashua",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68512",
      "recalling_firm": "Vascular Technology, Inc.",
      "address_1": "12 Murphy Dr",
      "address_2": "",
      "postal_code": "03062-1903",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - US including California and the countries of Australia, United Kingdom and Taiwan.",
      "recall_number": "Z-1999-2014",
      "product_description": "07-150-10 MIZUHO, DOPPLER PROBE, SLIM, BX 4, REF 138660    The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow.",
      "product_quantity": "147",
      "reason_for_recall": "Report of the product penetrating the sterile barrier; this  could render the product unsterile.",
      "recall_initiation_date": "20140528",
      "center_classification_date": "20140707",
      "termination_date": "20160211",
      "report_date": "20140716",
      "code_info": "LOT NUMBER 11802-37667",
      "more_code_info": ""
    }
  ]
}