ClearanceBrief
Recall Z-2801-2015 ยท JAK System, X-Ray, Tomography, Computed

GE Healthcare

Lightspeed 16 CT

DateSep 21, 2015 (initiated Jul 17, 2015)
StatusTerminated
ReasonPotential for expulsion of the Power Supply on Lightspeed CT scanner or Discovery ST PET CT or Discovery LS PET CT scanner.
Root causeProcess control
ActionGE Healthcare sent an "Urgent Medical Device Correction" letter to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. GE Healthcare will correct all affected products at no cost to you. A GE Healthcare representative will contact you to arrange for the correction. For questions contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative. Ref# 25463
Quantity416
DistributionWorldwide Distribution - US (nationwide) and to the countries of : ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, CANADA, CHINA, DENMARK, ESTONIA, FINLAND, FRANCE, GERMANY, HUNGRY, INDIA, INDONESIA, ISRAEL, ITALY, JAPAN, REPUBLIC OF KOREA, MEXICO, NORWAY, POLAND, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH A
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K013561LIGHTSPEED 4.0 CT SCANNER SYSTEM
GE Medical Systems, Nov 8, 2001
K030420LIGHTSPEED 5.0 COMPUTED TOMOGRAPHY SYSTEM
GE Medical Systems, Mar 10, 2003
K040172MODIFICATION TO GE DISCOVERY LS SYSTEM
GE Medical Systems, Apr 7, 2004