ClearanceBrief
Recall Z-2578-2018 ยท KPS System, Tomography, Computed, Emission

GE Healthcare, LLC

Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22

DateMay 24, 2018
StatusTerminated
ReasonSome CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
Root causeComponent change control
ActionGE Healthcare notified customers on about 05/24/2018 via URGENT MEDICAL DEVICE CORRECTION letter. The letter outlined the reason for recall and notified customers that a GE Healthcare representative would be contacting them to arrange for the correction of the devices. Any questions or concerns can be directed to GE Healthcare Service at 1-800-437-1171 or a local Service Representative.
Quantity42 devices total
DistributionNationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K141477DISCOVERY IQ
Ge Medical Systems, LLC, Sep 18, 2014