{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "97538",
      "product_res_number": "Z-0833-2012",
      "event_date_initiated": "2011-01-31",
      "event_date_posted": "2012-02-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-09-06",
      "res_event_number": "57842",
      "product_code": "RCE",
      "product_description": "GE eXplore Locus Micro CT cabinet x-ray system model RS9-80.\n\nCT Scanner for laboratory mice or other research.",
      "code_info": "Part Number 5134163.",
      "firm_fei_number": "2126677",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53188-1615",
      "additional_info_contact": "262-513-4122",
      "reason_for_recall": "Product fails to comply with the federal performance standard for cabinet x-ray systems (Title 21 CFR 1020.40(c)(1)(i)). Specifically, the x-ray emission limit of 0.5 milliroentgen in one hour could be exceed. Highest emission measured was 3 mR/hr.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "GE Healthcare will notify purchasers of the problem, the affected product, instructions for users, and specify the maximum emission rate measured.  GE Healthcare will bring defective systems into compliance free of charge. This will be done via Field Modification Instructions IFMI) 11101 which is scheduled for deployment on March 1, 2011 with an estimated completion date of July 1, 2011.",
      "product_quantity": "21",
      "distribution_pattern": "Worldwide Distribution",
      "openfda": {
        "device_name": "Cabinet X-Ray, Industrial",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
      }
    }
  ]
}