GE Medical Systems recalls Vivid E80, E90, and E95 ultrasound systems due to potential power cord breakage causing electrical shock. Affected units may need repair or replacement.
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 E80, E90, and E95 ultrasound systems because the power cord can break and expose electrical conductors, creating a shock hazard. This could lead to serious injury if the system is used improperly.
The power cord can break, exposing electrical conductors inside. This creates a risk of electrical shock if the system is touched or used while the cord is damaged. The hazard is specific to the power cord and not the entire system.
Healthcare providers and medical facilities using the Vivid E80, E90, or E95 ultrasound systems are most at risk. Patients and staff could be exposed to electrical shock if the power cord breaks.
Check for the Vivid E80, E90, or E95 ultrasound system models. These systems were sold for cardiac imaging, fetal monitoring, and other medical uses. Each unit has a unique serial number.
Inspect the power cord for any signs of damage or breakage that could expose electrical conductors.
Reach out to GE Medical Systems for a repair or replacement of the affected ultrasound system.
The power cord can break and expose electrical conductors, creating a risk of shock.
Vivid E80, E90, and E95 ultrasound systems.
Check for the Vivid E80, E90, or E95 model. Each unit has a unique serial number assigned.
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-2986-2018 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2986-2018 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.
