GE Medical Systems, LLC has recalled 25,616 Venue Go and Venue Fit diagnostic ultrasound systems because the internal battery can fail. This failure can cause the device to overheat, potentially resulting in smoke or fire. The recall affects models R2 through R5 distributed between various dates. GE Medical Systems has notified affected customers by letter and is coordinating corrective actions. Consumers should stop using the devices and contact the manufacturer directly to arrange for a return, replacement, or repair of the systems.
The internal battery in these ultrasound systems can experience a failure that leads to overheating, which can result in the device emitting smoke or catching fire. This poses a fire hazard and potential for injury to patients or medical personnel in clinical environments.
Stop using and coordinate return/correction with manufacturer.
Quantity: 12,808 total devices.
Quantity: 12,808 total systems.
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · Raw API Response
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