Lightspeed 16 CT
Check against the official notice below — it lists the full affected range.
GE Healthcare issued a recall affecting 416 units of Lightspeed CT scanners, Discovery ST PET CT scanners, and Discovery LS PET CT scanners due to a potential hazard where the power supply could be expelled from the equipment. The affected devices were distributed worldwide, including throughout the United States and to 29 additional countries including Canada, Australia, Japan, and numerous European nations. Multiple lot and code numbers are associated with this recall, identifying the specific units involved.
The recall record does not specify a remedy or corrective action for affected consumers to undertake.
Written by software from the official notice below. Not reviewed by a lawyer.
Potential for expulsion of the Power Supply on Lightspeed CT scanner or Discovery ST PET CT or Discovery LS PET CT scanner.
Reason for recall: Potential for expulsion of the Power Supply on Lightspeed CT scanner or Discovery ST PET CT or Discovery LS PET CT scanner. Distribution: Worldwide 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 AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN and UNITED KINGDOM. Quantity: 416 Lot/code info: 00000058433HM4 4860LS16GS FMI25463004 910213080 FMI25463005 910212101 FMI25463006 910212105 FMI25463007 910213064 FMI25463008 910216041 FMI25463009 910216036 00000321402CN0 910212106 00000325191CN5 AH5362CT02 FMI25463010 190020CT03 FMI25463011 110807CT01 00000980106YM9 110040CT03 00000307018CN2 416249LS16 00000298660CN2 204787LSPD2 00000318927CN1 514468BLS 00000329994CN8 819561LS 00000389961CN4 709891CT 00000335314CN1 514934CLS16 00000340630CN3 82421140148 00000331165CN1 82421010103 00000336002CN1 82421130067 00000334898CN4 82421140150 00000322331CN0 82421160145 00000999187YM8 82421100291 FMI25463133 828210047 FMI25463136 82421310073 00000989604YM4 82421030247 FMI25463015 82421010063 00000075153HM7 82421120171 FMI25463016 082421ATCLSP04 FMI25463017 82421100443 00000080677HM8 82421090111 00000092789HM7 82421120191 00000092771HM5 82421120188 00000074379HM9 82421060038 FMI25463018 82421130055 00000092530HM5 82421110048 00000080298HM3 82421100270 FMI25463019 395291CT01 FMI25463020 PM1633CT04 FMI25463021 PC7479CT02 FMI25463022 DK1025CT02 00000420281CN8 NP384114 FMI25463023 FI2000MN01 00000953833YM1 FI1052CT02 FMI25463024 C6010809 FMI25463025 M1076839 FMI25463026 M40345153 FMI25463027 M4496936 FMI25463028 M4409416 FMI25463029 M2147233 FMI25463030 M4505261 FMI25463031 M4020535 FMI25463032 M4491526 FMI25463033 M2802781 FMI25463034 X971285001 FMI25463035 A4463317 FMI25463036 B4195716 00000320672CN9 M4160064 00000271501CN9 M4182817 00000302750CN5 HC3314CT02 00000311056CN6 PC1268CT03 00
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.