Manufacturer
113 recalls in our database name GE Medical Systems, LLC as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
GE recalled Discovery MR750w MRI systems where planned maintenance checks for caster lock functionality may not have been performed. This affects 519 units distributed worldwide.
GE HealthCare recalled certain MRI systems after discovering that planned maintenance checks to verify caster lock functionality on patient tables may not have been performed on some units.
GE HealthCare recalls certain SIGNA MRI systems because planned maintenance checks on patient table caster locks may not have been completed. Multiple system models are affected, with systems that underwent maintenance since March 1, 2023 in scope.
GE HealthCare identified that maintenance steps to verify caster lock functionality on certain SIGNA MR patient tables may not have been performed. Affected healthcare facilities should contact GE HealthCare to verify their systems.
GE HealthCare issued a Class II recall for SIGNA MR imaging systems because planned maintenance to verify patient table caster lock functionality may not have been performed on certain units.
GE HealthCare is recalling certain MR imaging systems because planned maintenance steps to verify caster lock functionality may not have been performed. Worldwide distribution includes 760 units.
GE is recalling certain MR imaging systems because planned maintenance checks of caster locks on patient tables may not have been performed. Unchecked caster locks could allow table movement during imaging.
GE HealthCare recalled 758 units of SIGNA and related MRI systems worldwide because maintenance checks on patient table caster locks may not have been performed, creating risk of unwanted table movement during imaging.
GE HealthCare is recalling certain MRI systems because planned maintenance checks on patient table caster locks may not have been completed on systems serviced since March 1, 2023.
GE HealthCare is recalling certain MRI systems where planned maintenance checks of patient table caster locks may not have been performed. Patients should contact GE or their healthcare facility about past procedures on affected systems.
GE HealthCare recalled certain MR imaging systems because the planned maintenance steps to check caster lock functionality on the patient table may not have been performed. Affected systems include SIGNA PET/MR AIR Plus (China Only).
GE HealthCare is recalling SIGNA Voyager AIR MRI systems in China where planned maintenance checks on patient table caster locks may not have been performed. Faulty locks could allow the patient table to move unexpectedly during imaging.
GE HealthCare recalls certain SIGNA MRI systems because maintenance procedures to verify caster lock functionality on patient tables may not have been performed. Affected units underwent planned maintenance since March 1, 2023.
GE HealthCare is recalling certain MR imaging systems because maintenance steps to verify caster lock functionality on the patient table may not have been performed.
GE HealthCare recalled Discovery MR450 1.5T MRI systems due to planned maintenance checks on patient table caster locks that may not have been performed, potentially compromising table stability.
GE HealthCare's Discovery MR750w 3.0T MRI systems can produce excessive acoustic noise from gradient coils during scanning, potentially exceeding safe hearing protection limits.
GE HealthCare is recalling certain SIGNA Architect AIR MRI systems because gradient coils can produce acoustic noise exceeding 99dB during scanning, surpassing safe limits even with required hearing protection.
GE HealthCare is recalling SIGNA Architect MR system gradient coils that can produce acoustic noise exceeding 99dB during scanning, potentially surpassing international safety limits even with required hearing protection.
GE Medical Systems recalled SIGNA PET/MR imaging systems because gradient coils produce acoustic noise exceeding 99 decibels during scanning, surpassing established safety limits even with hearing protection.
GE Medical Systems is notifying healthcare facilities that certain OEC Elite and OEC 3D Mobile C-arm systems have X-ray field sizes exceeding the 4% Source to Image Distance specification. No illnesses or injuries have been reported.
GE Medical Systems is recalling OEC Elite and OEC 3D Mobile C-arm systems with potential X-ray field size issues. Some units may exceed the 4% Source-to-Image Distance limit or lack documented acceptance limits in their service manuals.
GE Medical Systems is recalling Venue Fit diagnostic ultrasound systems because the battery can potentially develop an internal failure causing smoke or fire. Approximately 12,808 systems have been distributed worldwide.
GE Medical Systems is recalling Venue Go ultrasound systems due to a battery defect that could cause smoke or fire. No injuries have been reported.
GE Healthcare Revolution CT systems may leak glycol coolant near the gantry base. While the non-toxic fluid poses no chemical hazard, it creates a slip-and-fall risk if not noticed and cleaned.
GE Healthcare Revolution Apex and Revolution CT series systems may leak coolant fluid onto the floor near the gantry. The blue-colored, non-toxic fluid poses a slip and fall hazard if not noticed.