GE Medical Systems recalls Vivid E95 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units sold to healthcare providers for medical imaging.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
GE Medical Systems is recalling Vivid E95 ultrasound systems because the power cord can break and expose electrical conductors, creating a shock hazard. This risk affects healthcare providers using the device for medical imaging.
The power cord on the Vivid E95 ultrasound system can break, exposing electrical conductors inside. This creates a risk of electric shock if the device is touched or handled improperly during use.
Healthcare providers who own or use the Vivid E95 ultrasound system for medical imaging are most at risk. The device is intended for qualified physicians performing ultrasound evaluations.
The Vivid E95 ultrasound system is sold to healthcare providers for medical imaging. Each unit has a unique serial number assigned to the consignee.
Inspect the power cord for any signs of damage or breakage that could expose electrical conductors.
Reach out to GE Medical Systems for guidance on whether the device needs repair or replacement.
The device may pose a shock risk if the power cord breaks, so it's recommended to check for damage and contact GE Medical Systems for further guidance.
The Vivid E95 ultrasound system is sold to healthcare providers for medical imaging, and each unit has a unique serial number assigned to the consignee.
Inspect the power cord for damage or breakage that could expose electrical conductors, and contact GE Medical Systems for guidance.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2988-2018 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2988-2018 from GE Medical Systems. 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.
