GE Vingmed recalls Vivid S60 ultrasound devices with software versions v203 or v204 that may delay boot-up, risking emergency response delays. Affected units must be checked for software version.
GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.
GE Vingmed is recalling Vivid S60 ultrasound devices with software versions v203 or v204 that may delay boot-up, potentially delaying emergency medical care. This could impact critical situations where quick ultrasound access is needed.
The device may fail to boot up quickly enough during emergencies, delaying access to ultrasound imaging. This could impact time-sensitive medical decisions, such as identifying life-threatening conditions in critical situations.
Healthcare providers using the Vivid S60 ultrasound device with software versions v203 or v204 are most at risk. Emergency medical staff who rely on this device for timely diagnostics could face delays in critical care.
Check the software version on your Vivid S60 device. Affected units have software versions v203 or v204. The device was sold with these specific software versions.
Review the software version on your Vivid S60 device to see if it is v203 or v204.
GE Healthcare has become aware that certain Vivid S60 ultrasound systems cannot boot up in a timely fashion, which may delay availability of the device in time-critical emergency situations.
Software versions v203 and v204 are affected.
No action is needed if your device has a different software version.
We’ve drafted a message you can send GE Vingmed to request your refund or repair — edit it as you like.
Subject: Recall Z-2124-2023 — GE Vingmed GE Vingmed Hello, I own a GE Vingmed that is covered by recall Z-2124-2023 from GE Vingmed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
