ClearanceBrief
Recall Z-0816-2022 ยท JAK System, X-Ray, Tomography, Computed

GE Healthcare, LLC

Revolution CT, Revolution CT ES

DateApr 5, 2022 (initiated Jun 30, 2021)
StatusOpen, Classified
ReasonThe accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
Root causeRadiation Control for Health and Safety Act
ActionGE Healthcare sent an Important Electronic Product Radiation Warning letter dated February 8, 2022 to all affected systems informing its users of the potential for the issue to occur and instruct the users as to what actions to take. 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, the details of which will be included in a subsequent communication to you or through a GE Healthcare field engineer site visit. For questions co
Quantity273 (51 US; 222 OUS) in total
DistributionWorldwide - US Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K133705REVOLUTION CT
Ge Medical Systems, LLC, Apr 11, 2014
K163213Revolution CT
Ge Medical Systems, LLC, Dec 16, 2016
K191777Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
Ge Medical Systems, LLC, Jul 26, 2019