{
  "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": "2026-07-08",
    "results": {
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      "status": "Ongoing",
      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97668",
      "recalling_firm": "UIH Technologies LLC",
      "address_1": "9380 Kirby Dr",
      "address_2": "",
      "postal_code": "77054-2515",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "recall_number": "Z-0221-2026",
      "product_description": "Shanghai United Imaging Healthcare Co., Ltd.   Computed Tomography X-ray System,   Model:uCT ATLAS  MD, Rx Only",
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      "reason_for_recall": "Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.",
      "recall_initiation_date": "20250912",
      "center_classification_date": "20251021",
      "report_date": "20251029",
      "code_info": "UDI: (01)06971576831104/ Serial Numbers: 863001, 863002",
      "more_code_info": ""
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}