{
  "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": "5 units",
      "code_info": "System :     S/N :                Model:  722013 262 Allura Xper FD20 BIPLANE R7.6  722013 422 Allura Xper FD20 BIPLANE R7.7  722013 195 Allura Xper FD20 BIPLANE R7.8  722013 173 Allura Xper FD20 BIPLANE R7.9  722013 225 Allura Xper FD20 BIPLANE R7.10",
      "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 Allure BiPlane Series:  Model              722013\tAllura Xper FD20 BIPLANE R7.6  722013\tAllura Xper FD20 BIPLANE R7.7  722013\tAllura Xper FD20 BIPLANE R7.8  722013\tAllura Xper FD20 BIPLANE R7.9  722013\tAllura Xper FD20 BIPLANE R7.10    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-0347-2016",
      "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"
    }
  ]
}