{
  "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": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98940",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to California.",
      "recall_number": "Z-2354-2026",
      "product_description": "DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.",
      "product_quantity": "1 unit",
      "reason_for_recall": "System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.",
      "recall_initiation_date": "20260501",
      "center_classification_date": "20260605",
      "report_date": "20260617",
      "code_info": "Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049."
    }
  ]
}