{
  "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": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "Monitor Ceiling Suspension system may fall",
      "address_2": "",
      "product_quantity": "9 units",
      "code_info": "System :     S/N :                Model:  722003 30 Allura Xper FD10  722010 670 Allura Xper FD10  722011 167 Allura Xper FD10/10  722012 1951 Allura Xper FD20  722012 536 Allura Xper FD21  722012 504 Allura Xper FD22  722012 748 Allura Xper FD23  722012 536 Allura Xper FD24  722012 579 Allura Xper FD25",
      "center_classification_date": "20151130",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the countries of: Canada,Australia, Austria, Brazil, Chile, China, Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, South Africa, Spain, Switzerland and United Kingdom.",
      "state": "MA",
      "product_description": "Philips Healthcare Allura Xper Series:  Allura Xper FD10  Allura Xper FD10/10  Allura Xper FD20  Allura Xper FD21  Allura Xper FD22  Allura Xper FD23  Allura Xper FD24  Allura Xper FD25    Product  Usage:  The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and thrombolysis and atherectomics), pacemaker Implantations and electrophysiology (EP). Use of the Allura Xper series system in the OR environment is restricted; the system should only be used for endo-vascular procedures. The Philips Integris Allura 9F is intended for diagnostic cardiovascular, vascular and interventional procedures",
      "report_date": "20151209",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems, Inc.",
      "recall_number": "Z-0346-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "70370",
      "termination_date": "20170118",
      "more_code_info": "",
      "recall_initiation_date": "20150203",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}