{
  "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": "Terminated",
      "city": "Shanghai",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90104",
      "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": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of TX.",
      "recall_number": "Z-1075-2022",
      "product_description": "Digital Medical X-ray Imaging System, Model: uDR 596i, uDR 592h",
      "product_quantity": "4",
      "reason_for_recall": "X-ray imaging system positioning image and protocol label is reversed for Flexion and Extension on C-Spine and L-Spine, this will cause the image to be incorrectly labeled and may cause the patient to have a repeat exposure.",
      "recall_initiation_date": "20190730",
      "center_classification_date": "20220512",
      "termination_date": "20220517",
      "report_date": "20220518",
      "code_info": "DI/GTIN: 06971576833023, Serial Numbers: 270012, 270013,270014, 270015"
    }
  ]
}