Every recall we track for GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING — 41 in all — plus the complaints and injury reports the public filed about them.
GE Medical Systems Israel recalls Omni Legend PET scanners (15cm, 16cm, 21cm, 32cm models) due to potential streaking artifacts in PET clinical scans. Affected units have specific UDI and manufacturing lot numbers listed in the recall.
GE Medical Systems Israel recalls certain Maxxus nuclear medicine systems that may have been moved without proper detector support, risking detector falls and serious injury. No injuries reported.
GE Medical Systems Israel recalls certain nuclear medicine systems that could have detector falls leading to injury. No injuries reported. Affected units are older models past end of guaranteed service.
GE Medical Systems Israel recalls certain SMV BodyTrack nuclear medicine systems that may have been moved without proper detector support, risking detector falls and serious injury. No injuries reported.
GE Medical Systems Israel recalls certain nuclear medicine systems that may have been moved without proper detector support, risking detector falls and injury. No injuries reported.
GE Medical Systems Israel recalls Optima NX cardiac gamma cameras due to potential detector falls causing serious injury if improperly relocated. Affected units have serial numbers in distribution.
GE Medical Systems Israel recalls Maxic: dual-head cardiac gamma cameras with serial numbers in distribution due to potential detector fall risk. Affected units may need repair or replacement to prevent injury.
GE Medical Systems Israel recalls Elsc: dual-head cardiac gamma cameras with serial numbers in distribution due to potential detector fall risk. Affected units may need repair or replacement to prevent injury.
GE Medical Systems Israel recalls Millennium MPS cardiac gamma cameras due to potential detector fall risk from improper relocation. Affected units may need repair or replacement to prevent serious injury.
GE Medical Systems Israel recalls Elscint Varicam cardiac gamma cameras that may have been moved without proper detector support, risking detector falls and serious injury.
GE Medical Systems Israel recalls Elscint SPX:4 dual-head cardiac gamma cameras that may have been moved without proper detector support, risking detector falls and serious injury.
GE Medical Systems Israel recalls Sopha Medical Vision (SMV) DSXi/DST-XLi, DST-XL, and DSTi gamma cameras. These dual-head nuclear medicine systems may have detector falls causing life-threatening injury if improperly relocated.
GE Medical Systems Israel recalls Elsc: Helix dual-head cardiac gamma cameras due to potential detector fall causing life-threatening injury if improperly relocated.
GE Medical Systems Israel recalls Starcam/Cam: dual-head cardiac imaging cameras with outdated detector support that could fall, causing injury. Affected units have serial numbers in distribution.
GE Medical Systems Israel recalls Millennium Myos: dual-head cardiac gamma cameras with serial numbers in distribution due to potential detector fall risk if improperly relocated.
GE Medical Systems Israel recalls Millennium MG/MC cardiac gamma cameras that may have been moved without proper detector support, risking detector falls and serious injury. Affected units include all serial numbers in distribution.
GE Medical Systems Israel recalls Elscint Model 4XX cardiac gamma cameras due to potential detector fall risk from improper relocation. Affected units may require repair or replacement to prevent serious injury.
GE Medical Systems Israel recalls Millennium MPR dual-head nuclear medicine gamma cameras due to potential detector fall risk if improperly relocated. Affected units may require repair or replacement to prevent serious injury.
GE Medical Systems Israel recalls Elscint SPX: dual-head cardiac gamma cameras with serial numbers in distribution due to potential detector fall risk. Affected units may need repair or replacement to prevent serious injury.
GE Medical Systems Israel recalls specific nuclear medicine scanners due to potential life-threatening motion during patient scans if software is outdated. Affected models include Varicam, Millennium VG, and Discovery VH systems with listed serial numbers.
GE Medical Systems Israel recalls Infinia, Infinia Hawkeye, Infinia II, and Infinia II Hawkeye 4 nuclear medicine systems with incorrect gantry software that may cause life-threatening injury during patient scans.
GE Healthcare recalls specific Varicam Millennium VG Discovery VH models due to potential detector fall risk if improperly supported. Affected units may cause serious injury if relocated without proper detector support.
GE Healthcare Discovery NM/CT 670 PRO models with specific serial numbers may have been moved without proper detector support, risking detector falls and serious injury. Affected units include models H2401AK, H2402AC, H3100AH, H3100XB, and 5376204-70-54-2.
GE Healthcare recalls Discovery NM 630 systems with specific model numbers due to potential detector fall risk during transport or relocation without proper support. This could lead to life-threatening injury. Affected units include models H2401CF, H2401CH, H2401JE, H3100JY, and 5376204-30-2.
GE Healthcare recalls Infinia II Hawkeye 4 models H2799PP, H2799PR, H2799YC, H2799YD, H3000WC and others due to potential detector fall from improper relocation. This could lead to life-threatening injury. Affected units have specific serial numbers and system IDs.
GE Healthcare recalls Optima NM/CT 640 nuclear medicine systems with certain serial numbers due to potential detector fall risk from improper relocation. Affected units may require inspection or repair to prevent serious injury.
GE Healthcare recalls certain Infinia II nuclear medicine systems (model numbers H2799ZP and H3000WT) that could have been moved without proper detector support, potentially causing detector falls and serious injury.
GE Healthcare recalls Infinia I Hawkeye 1 models H3000WN, H3000YM, H3000YS due to potential detector fall risk from improper relocation. Affected units may need inspection or repair.
GE Healthcare Discovery NM/CT 670 models H2401BC, H2401CE, H2401CG, H3100AG, H3100JW, H3100NC may have been transported without proper detector support, risking detector falls and serious injury. Affected units include specific model numbers and serial numbers.
GE Medical Systems Israel recalls Discovery NM/CT 670 ES models with specific serial numbers due to potential detector fall risk from improper transport. Affected units may cause life-threatening injury if detector mounts are damaged.
GE Healthcare is recalling certain Discovery NM/CT 670 DR systems that may have been moved without proper detector support, risking detector falls and serious injury.
GE Medical Systems Israel recalls Discovery NM/CT 670 CZT systems with specific model numbers due to potential detector fall risk if improperly relocated. Affected units may require inspection to prevent life-threatening injury.
GE Medical Systems Israel recalls specific Infinia I nuclear medicine systems (models 5178728, H3000WE, H3000WM, H3000YG) due to potential detector fall causing serious injury if improperly relocated.
GE Healthcare recalls Brivo NM 615 nuclear medicine systems with specific model numbers due to potential detector fall risk from improper relocation. Affected units may cause life-threatening injury if detector falls.
GE Medical Systems Israel recalls specific MyoSPECT cardiac SPECT systems due to potential service handle loosening that could cause injury to service personnel from falling covers.
GE Medical Systems Israel recalls specific GE Nuclear Medicine 600/800 series systems due to potential detector fall causing life-threatening injury. Affected models include 870, 870 DR variants, and D670 series with certain serial numbers.
GE Medical Systems Israel recalls specific nuclear medicine imaging systems due to risk of detector falling and causing serious injury if mitigation isn't properly implemented.
GE Medical Systems Israel recalls specific GE Nuclear Medicine 600/800 series systems (850, 850/Dismount, 850 3/8 inch NM Gantry, 860 models) due to risk of detector falling and causing life-threatening injury. Affected units have serial numbers listed in the recall notice.
GE Medical Systems Israel recalls specific nuclear medicine imaging systems due to potential detector fall causing life-threatening injury. Affected models include 870 CZT O540+ and D670 CZT gantries with serial numbers listed.
GE Medical Systems Israel recalls specific GE Nuclear Medicine 600/800 series systems where a detector may fall, causing life-threatening injury. Affected models include 830 variants with certain serial numbers and configurations.
GE Medical Systems Israel recalls specific GE Nuclear Medicine 600/800 series systems due to potential detector fall causing life-threatening injury. Affected models include BRIVO B615 variants with certain serial numbers.
