{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Shanghai",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85868",
      "recalling_firm": "Shanghai United Imaging Healthcare Co., Ltd.",
      "address_1": "No. 2258 Chengbei Rd, Jiading Ind.",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution including in the states of CA, IN and TX. See uploaded distribution list for more details.",
      "recall_number": "Z-2703-2020",
      "product_description": "Computed Tomography X-ray System; Model uCT 760; Rx;  UDI: (01) GTIN: 06971576831043 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body (including head, neck, cardiac, and vascular).",
      "product_quantity": "5 units",
      "reason_for_recall": "The metal edge overlap of the mylar strip in the gantry was uneven, which may create a sharp edge.",
      "recall_initiation_date": "20200620",
      "center_classification_date": "20200727",
      "report_date": "20200805",
      "code_info": "SN 600229, 600230, 600232, 600271, 600282"
    }
  ]
}