{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Best",
      "state": "",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99223",
      "recalling_firm": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.",
      "address_1": "Veenpluis 4-6",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "",
      "distribution_pattern": "US and ROW.",
      "recall_number": "Z-2411-2026",
      "product_description": "Philips MultiDiagnost Eleva with the following Model Numbers:    Model # 708032 for MultiDiagnost Eleva;  Model # 708034 for MultiDiagnost Eleva with Flat Detector;  Model # 708036 for MultiDiagnost Eleva;  Model # 708037 for MultiDiagnost Eleva with Flat Detector;  Model # 708038 for MultiDiagnost Eleva with Flat Detector.",
      "product_quantity": "",
      "reason_for_recall": "Philips Allura Xper and MultiDiagnost-Eleva systems  Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended  radiation exposure and additional contrast injection",
      "recall_initiation_date": "20260518",
      "center_classification_date": "20260616",
      "report_date": "20260624",
      "code_info": "All codes",
      "more_code_info": ""
    }
  ]
}