{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Suzhou",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99511",
      "recalling_firm": "Philips Healthcare (Suzhou) Co., Ltd.",
      "address_1": "Suzhou Industrial Park",
      "address_2": "No. 258 Zhongyuan Road; Pingjiang",
      "postal_code": "N/A",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "U.S. Nationwide and U.S. Territories distribution.",
      "recall_number": "Z-2988-2026",
      "product_description": "Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.",
      "product_quantity": "N/A",
      "reason_for_recall": "Potential of failing to trigger clinical scan during Bolus Tracking.",
      "recall_initiation_date": "20260626",
      "center_classification_date": "20260821",
      "report_date": "20260902",
      "code_info": "Device Identifier: (01)00884838085015, (01)00884838105508."
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}