{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Shanghai",
      "state": "",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87289",
      "recalling_firm": "Shanghai United Imaging Healthcare Co., Ltd.",
      "address_1": "No. 2258 Chengbei Rd, Jiading Ind.",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of TX.",
      "recall_number": "Z-1160-2021",
      "product_description": "Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, limbs and trunk. Not for mammography.",
      "product_quantity": "6 units",
      "reason_for_recall": "There is a potential for  the X-Ray tube head (Touch screen interface) to perform an uncommanded motion.  This could result in a collision with the patient.",
      "recall_initiation_date": "20210125",
      "center_classification_date": "20210302",
      "termination_date": "20220503",
      "report_date": "20210310",
      "code_info": "Serial Number: 270012, 270013, 270014, 270015, 270016, 270017",
      "more_code_info": ""
    }
  ]
}