Every recall we track for GE Healthcare LLC — 283 in all — plus the complaints and injury reports the public filed about them.
GE Healthcare recalls SIGNA Premier MRI systems that may have steel fittings instead of brass, which could attract during service and cause injury if magnet is ramped.
GE Healthcare recalls specific versions of Centricity Universal Viewer software due to inaccurate distance and area measurements when using Global Stack viewport. Affected units include models 2088026-9XX and 5826659-0XX.
GE Healthcare recalls SIGNA Premier MRI scanners (model 5748519) due to rare risk of hearing loss from elevated acoustic noise during scans. Affected units have specific GTINs.
GE Healthcare recalls Centricity PACS software version 7.0 SP0.0.4.7 due to failure to process study modification notifications on post-verified exams. Affected units include model 5831882-012 with GTIN 00840682145572.
GE Healthcare recalls Centric: Universal Viewer Zero Footprint software versions 6.0 SP6 to SP11.4 due to potential inaccurate medical image measurements. Affected users should contact GE for details.
GE Healthcare recalls service manuals for CT, PET, and NM tables that may cause injury if service personnel remove wrong screws without proper table supports.
GE Healthcare recalls Aisys CS2 and Avance CS2 anesthesia systems with specific serial numbers due to potential reversal of oxygen and air pressure transducer connections.
GE Healthcare recalls Avance CS2 and Aisys CS2 anesthesia systems with a crack risk in the base that could cause falls. Affected units have specific serial numbers and GTINs. Contact GE Healthcare for details.
GE Healthcare recalls CARESCAPE Central Station V2 models 2082278-001 and 2082279-001 due to potential power supply failure causing loss of patient monitoring. Affected units include specific display and component parts.
GE Healthcare recalls Centricity PACS RA1000 software versions 3.0-3.2 SP8, 4.0-4.0 SP14, 6.0-6.0 SP10.3, and 7.0-7.0 SP0.0.4.7 due to potential inaccurate distance and area measurements when viewing magnified or scaled-down images.
GE Healthcare recalls Centricity Cardiology CA1000 software versions 1.0 to 1.0 SP and 2.0 to 2.0 SP14H due to potential inaccurate distance and area measurements when using magnified or scaled-down images.
GE Healthcare recalls Centricity Enterprise Web software versions 3.0-3.0 SP14d, 4.0-4.0 SPa6c and 4.0 SPa7b due to potential inaccurate distance and area measurements when using magnified images or lossy scaled-down images.
GE Healthcare recalls Centric: Universal Viewer Zero Footprint Client software versions 6.0 SP11 through 6.0 SP11.4 due to potential inaccurate distance and area measurements on magnified or scaled-down images.
GE Healthcare recalls Centricity Radiology RA600 software versions 7.0-7.0 SP and 8.0-8.0 SP14H due to potential inaccurate distance and area measurements on magnified or scaled-down images. Affected units may require software update.
GE Healthcare recalls backup batteries installed on or after April 1, 2019 for Avance anesthesia devices due to potential early failure. Affected units may need replacement to prevent unexpected shutdowns.
GE Healthcare recalls Avance CS2 and CS2 Pro anesthesia devices manufactured on or after April 1, 2019, due to backup batteries failing earlier than expected. Affected units have specific serial numbers and model numbers listed in the recall.
GE Healthcare recalls ventilators with insufficient battery backup that may shut down prematurely when not connected to AC power. Affected models include CARESCAPE R860 and ENGSTROM series with specific serial numbers. Stop using immediately to prevent life-threatening shutdowns.
GE Healthcare recalls replacement backup batteries for CARESCAPE R860 and Engström Carestations distributed after April 1, 2019, due to risk of ventilator shutdown without AC power.
GE Healthcare recalls specific MUSE Cardiology Information System models due to risk of lost test measurements and diagnosis statements after signing in the web client. Affected units have unique serial numbers and model identifiers.
GE Healthcare is recalling several MRI systems due to a risk of magnet falling during de-installation if hardware isn't properly secured, potentially causing injury. Affected models include SIGNA Premier, SIGNA Architect, SIGNA Pioneer, Discovery, and others. No remedy is specified in the recall notice.
GE Healthcare recalls 1.5T and 3.0T SIGNA HDx, HDxt, and HDxt Mobile MRI systems due to potential image flipping left to right. Affected units have specific system IDs listed in the recall notice.
GE Healthcare recalls 1.5T and 3.0T SIGNA Excite HD MRI systems due to potential left-right image flipping. Affected units have specific system IDs listed in the recall notice.
GE Healthcare recalls SIGNA Excite 3T MRI systems due to potential left-right image flipping. Affected units have specific system IDs listed in the recall notice. Consumers should contact GE for details.
GE Healthcare recalls Signa 1.5T TwinSpeed MRI systems due to potential left-right image flips. Affected units have specific system IDs listed in the recall notice.
GE Healthcare recalls v2.0 Central Station models with unapproved keyboards that may mute alarms, risking missed critical alerts. Affected units include specific serial numbers and versions.
GE Healthcare recalls 1.5T and 3.0T MRI systems due to potential cryogen ventilation system failures. Affected units may not meet venting requirements, but no injuries reported. Consumers should contact GE for details.
GE Healthcare recalls SIGNA Horizon Cx, Horizon Lx, Infinity, MR/I, SmartSpeed, EchoSpeed Plus, and HighSpeed Plus MRI systems due to potential cryogen ventilation system failures. Affected units may require repair to prevent safety hazards.
GE Healthcare recalls SIGNA MR355 and MR36: Cryogen ventilation systems may not meet venting requirements. Affected units require inspection by authorized personnel.
GE Healthcare recalls SIGNA Premier MRI systems due to potential cryogen ventilation system failures. This could lead to unsafe conditions in the imaging environment.
GE Healthcare recalls Discovery MR450 1.5T MRI systems due to potential cryogen ventilation system failures. This could lead to unsafe conditions in the imaging environment.
GE Healthcare recalls Optima MR450w 1.5T MRI systems due to potential cryogen ventilation system failures. Affected units may require repair or replacement to prevent safety risks.
GE Healthcare recalls Brivo MR355 MRI systems due to potential cryogen ventilation system failures. Affected units may require safety checks to prevent risks.
GE Healthcare recalls SIGNA HFO/I MRI systems due to potential cryogen ventilation system failures. Affected units may require repair to prevent safety risks.
GE Healthcare recalls SIGNA Infinity MR systems due to potential cryogen ventilation system failures. This could lead to unsafe conditions during MRI scans. Affected units may require inspection or repair.
GE Healthcare recalls MR MAX System superconducting magnets due to potential cryogen ventilation system failures. This could lead to unsafe conditions in the imaging environment.
GE Healthcare recalls 3.0T SIGNA Infinity TwinSpeed MRI systems due to potential cryogen ventilation system failure. Affected units may require repair or replacement to prevent safety risks.
GE Healthcare recalls 1.5T and 3.0T MRI systems due to potential cryogen ventilation system failures. Affected units may pose risks if not properly vented.
GE Healthcare recalls 1.5T SIGNA HDe MRI systems due to potential cryogen ventilation system failures. This could lead to unsafe conditions in the imaging environment.
GE Healthcare recalls SIGNA Pioneer MRI systems due to potential cryogen ventilation issues. Affected units may not meet venting requirements, posing safety risks.
GE Healthcare recalls 0.7T SIGN: Venting issue in MRI systems may cause safety risks. Affected units require immediate action.
GE Healthcare recalls SIGNA Architect MRI magnets due to potential cryogen ventilation system issues. Affected units may not meet venting requirements.
GE Healthcare recalls SIGNA Voyager and Premier Edition MRI magnets due to potential cryogen ventilation system failure. Affected units may require repair or replacement to prevent safety risks.
GE Healthcare recalls SIGNA 3.0T MRI systems due to potential cryogen ventilation system failures. This could lead to unsafe conditions in the imaging environment.
GE Healthcare recalls SIGNA 1.5T TwinSpeed MR systems due to potential cryogen ventilation system failures. Affected units may have unsafe venting that could lead to health risks.
GE Healthcare recalls SIGNA Artist MRI system magnets due to potential cryogen ventilation system failure. Affected units may not meet venting requirements.
GE Healthcare recalls Vscan Extend devices sold as 'Vscan Extend Dual DICOM' due to battery depletion causing failure to power on when not properly turned off or connected to computer without AC power. Affected units have specific serial numbers listed in the recall.
GE Healthcare recalls Vscan Extend consoles with serial numbers ending in 5693455 due to battery depletion when not properly turned off before removal or computer connection without AC power.
GE Healthcare recalls Vscan Extend devices sold as 'Vscan Extend Sector Wi-Fi' that won't power on due to battery issues when not turned off before removal or computer connection without AC power.
