Revolution CT, Revolution CT ES
- Company
- Ge Healthcare, Llc
- Recall Initiated
- June 30, 2021
- Posted
- April 5, 2022
- Recall Number
- Z-0816-2022
- Quantity
- 273 (51 US; 222 OUS) in total
- Firm Location
- Waukesha, WI
Reason for Recall
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
Distribution
Worldwide - US Nationwide distribution.
Lot / Code Info
Revolution CT, Revolution CT ES
Root Cause
Radiation Control for Health and Safety Act
Action Taken
GE 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 contact GE Healthcare Services at 1 (800) 437-1171 or local Service Representative.