{ "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": "2026-08-15", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "112315", "product_res_number": "Z-0115-2013", "event_date_initiated": "2011-12-20", "event_date_posted": "2012-10-17", "recall_status": "Terminated", "event_date_terminated": "2013-09-18", "res_event_number": "63027", "product_code": "IZI", "product_description": "GE Healthcare innova 3131-IQ Mobile X-ray system.\n\nThe innova systems are indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional procedures, and optionally , rotational angiography procedures. They are also indicated for generating fluoroscopic images of human anatomy for cardiology, diagnostic, and interventional procedures.", "code_info": "Model number - 5892935G052G", "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": "It was discovered of a potential failure of the spectral filter mechanism inside the collimator of the innova 3100, innova 3100-IQ and innova 3131-IQ systems.", "root_cause_description": "Radiation Control for Health and Safety Act", "action": "GE Healthcare will, without charge, remedy the defect or bring the product into compliance with each applicable Federal standard in accordance with a plan to be approved by the Secretary of Health and Human Services. \n\nA GE Healthcare Service Representative will replace the collimator to address the issue.\n\nNotification of all dealers and purchasers is to be made within 15 working days of receipt of this letter in the manner specified in 21 CFR 1003.21 and 1003.22. \n\nThis office and the Food and Drug Administration (FDA) district office coordinator noted below are to be included in the notification. \n\nFurther questions please call 262-513-4122.", "product_quantity": "199 installed in the US", "distribution_pattern": "Nationwide distribution", "openfda": { "k_number": [ "K941979", "K932410", "K073328", "K955179", "K903373", "K222240", "K970525", "K073290", "K100371", "K042646", "K073088", "K991231", "K903371", "K936002", "K943545", "K910654", "K061871", "K905518", "K113034", "K042961", "K023441", "K052039", "K010721", "K896088", "K133719", "K052076", "K933460", "K903493", "K100468", "K100849", "K243077", "K945375", "K910370", "K923813", "K202391", "K231986", "K924719", "K111209", "K853044", "K945293", "K972136", "K060749", "K032443", "K162991", "K071037", "K884008", "K030139", "K972655", "K954309", 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