{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Westwood",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65158",
      "recalling_firm": "Medical Information Technology, Inc.",
      "address_1": "Meditech Circle",
      "address_2": "N/A",
      "postal_code": "02090",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA, including Puerto Rico and the country of Canada.",
      "recall_number": "Z-1365-2013",
      "product_description": "MEDITECH Bi-Directional interactive Communication Analyzer Interface;     Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.",
      "product_quantity": "56 devices",
      "reason_for_recall": "Incorrect transmission of laboratory results.",
      "recall_initiation_date": "20130507",
      "center_classification_date": "20130522",
      "termination_date": "20141001",
      "report_date": "20130529",
      "code_info": "Magic Releases 5.41, 5.52. 5.53, 5.62, 5.63, 5.64 and Client Server Releases 5.64, 5.65, 6.05, 6.06, 6.07"
    }
  ]
}