{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Road",
      "reason_for_recall": "Creepage Distance between the two primary phases in the GEO Transformer is 4.5 mm.does not meet (IEC)  International standard of 5.5 mm.",
      "address_2": "",
      "product_quantity": "4 systems",
      "code_info": "Lot or Serial Numbers   With affected M-cabinet CXA;   Serial number; 11-K0003;   12-B0001, 12-B0002; 12-B0003",
      "center_classification_date": "20120914",
      "distribution_pattern": "Worldwide Distribution - USA including OH and WA and the country of Canada",
      "state": "MA",
      "product_description": "Philips DigitalDiagnost Systems with M Cabinet   Model: 712025    Stationary radiographic system, digital-Universal RAD Applications",
      "report_date": "20120926",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Inc.",
      "recall_number": "Z-2384-2012",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "62884",
      "termination_date": "20170117",
      "more_code_info": "",
      "recall_initiation_date": "20120814",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}