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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

4 recalls · page 1 of 1

Medical devices

Reported Mar 5, 2025

SIGNA Creator, SIGNA Explorer, NMRI systems

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare (China) Co., Ltd.

Matched: BrandFor certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR…

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 11, 2024

GE Healthcare Discovery RT, Model Number 2374681-17, X-ray/computed tomography systems labeled as:

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare (China) Co., Ltd.

Matched: Brand · Product · Product details · Reason for recallGE HealthCare has become aware of a potential issue on certain Discovery, Optima, Revolution series CT systems, and certain operator console upgrades…

16 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 4, 2024

GE Proteus XR/A radiographic system

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare (China) Co., Ltd.

Matched: Brand · Product · Product details · Reason for recallSteel cables in the Wall Stand for certain Proteus XR/a systems serviced by GE HealthCare have not been replaced at the intervals detailed in the…

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

GE Healthcare Proteus XR/a, stationary X-Ray System, Model/Catalog Numbers: 1) 2259973; 2) 2259988; 3) 2266999; 4)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare (China) Co., Ltd.

Matched: Brand · Product · Product detailsThe XR system, Proteus XR/a, does not have a de-installation manual describing process steps for de-installing the devices. De-installation…

FDA (openFDA device enforcement)

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