{
  "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": "2026-04-22",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "Philips had discovered  through a field service testing where a device failed to comply with a Federal standard.",
      "address_2": "",
      "product_quantity": "one system",
      "code_info": "Model Number: Integris Allura 15-12  Serial Number: 16741023",
      "center_classification_date": "20141009",
      "distribution_pattern": "US distribution to FL",
      "state": "MA",
      "product_description": "Philips Healthcare Integris Allura 15 -12   Fluoroscopy x ray system",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems, Inc.",
      "recall_number": "Z-0022-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69197",
      "termination_date": "20141203",
      "more_code_info": "",
      "recall_initiation_date": "20140808",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}