Manufacturer
475 recalls in our database name GE Healthcare, LLC as the manufacturing or recalling firm.
Of the 475 recalls from GE Healthcare, LLC we have scored against our rubric, 8 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 43 (9%) are Severe.
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 Healthcare is recalling 10,884 Lightspeed RT16 X-ray systems because a defect may cause scans to start before a prescribed delay completes.
GE Healthcare is recalling Discovery NM/CT 670 X-ray systems because a defect may cause scans to start before a prescribed delay completes.
GE Healthcare is recalling 2,380 patient steps for RFX, Legacy, and Precision 500D systems because they may detach from the table, posing a fall risk.
GE Healthcare is recalling Vivid Ultrasound systems because slow search times can cause operators to select the wrong patient, potentially leading to misdiagnosis.
GE Healthcare is recalling Vivid E95, E90, and E80 ultrasound systems because slow search times can cause operators to select the wrong patient, potentially leading to misdiagnosis.
GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.
GE Healthcare is recalling Infant Warmer Systems because loose screws in the Heater Head could fall and cause thermal injury to patients.
GE Healthcare is recalling RFX and other systems because aged CRT monitors may fall. This poses a risk of injury or property damage.
GE Healthcare is recalling ADVANTX LCA and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and internationally.
GE Healthcare is recalling Precision 500D and other systems because aged CRT monitors may fall.
GE Healthcare is recalling specific CRT monitors due to a risk that aged units may fall. The recall affects multiple imaging system models.
GE Healthcare is recalling specific X-ray systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling Innova 2000 and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
GE Healthcare is recalling Prestige VH and other medical systems because aged CRT monitors may fall.
GE Healthcare is recalling ADVANTX LCV+ systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling Legacy and other imaging systems because aged CRT monitors may fall. The recall covers 1,598 units distributed in the US and internationally.
GE Healthcare is recalling Prestilix and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
GE Healthcare is recalling Prestige II and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and abroad.
GE Healthcare is recalling Prestige SI and other systems because aged CRT monitors may fall. The recall covers 1,598 units in the US and overseas.
GE Healthcare is recalling specific CRT monitors due to the potential for the units to fall. The recall affects multiple system models including ADVANTX and Prestige.
GE Healthcare is recalling specific Avance CS2, Avance, and Amingo anesthesia devices because they may enter a System Malfunction state if a storage drawer closes with excessive force.
GE Healthcare is recalling SIGNA Creator and SIGNA Explorer MRI scanners due to an incorrect RF Power Monitor Function that could cause higher than expected thermal dose and localized heating to patients.
GE Healthcare is recalling 471 Discovery MR750w MRI scanners because a small area of the patient bore can become warm enough to cause a serious burn if proper padding is not used.
GE Healthcare is recalling 97 MSK 1.5T Extreme MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
GE Healthcare is recalling 101 Optima 1.5T MR430s MR Scanners because gas venting may not occur properly, posing a risk of oxygen deprivation.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
GE HealthCare
American multinational medical technology company
Source: Wikidata (Q1152374), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.