GE Medical Systems recalls Vivid E9 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking 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 E9 ultrasound systems because the power cord can break and expose electrical conductors, creating a shock hazard. This risk affects medical professionals and facilities using the device for imaging.
The power cord on the Vivid E9 ultrasound system can break, exposing electrical conductors inside. This could lead to electric shock if someone touches the exposed wires while the device is in use.
Medical professionals and healthcare facilities that use the GE Vivid E:9 ultrasound system for imaging are most at risk. The device is intended for use by qualified physicians or under their direction.
The GE Vivid E9 ultrasound system is a general-purpose imaging device used for cardiac, fetal, abdominal, and other medical imaging. Check the serial number on the device or its packaging for the specific model.
Inspect the power cord for any signs of damage or fraying before use.
If the power cord is damaged, contact GE Medical Systems for repair or replacement options.
This recall applies to GE Vivid E9 ultrasound systems used for medical imaging. Check your device's serial number to confirm if it's affected.
Contact GE Medical Systems directly for repair or replacement options if your power cord is damaged.
The recall does not specify a deadline for action, but you should address any power cord damage immediately to prevent shock risks.
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-2985-2018 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2985-2018 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.
