GE Medical Systems recalls LOGIQ E9 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units were 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 its LOGIQ E9 ultrasound systems because the power cord can break and expose electrical conductors, creating a shock hazard. This risk is serious as the device is used by qualified physicians for medical imaging.
The power cord on the GE LOGIQ E9 ultrasound system can break, exposing electrical conductors inside. This creates a risk of electric shock if the device is touched or handled improperly during medical procedures.
Healthcare providers who own or use the GE LOGIQ E:9 ultrasound systems for medical imaging are most at risk. The device is intended for use by qualified physicians in clinical settings.
The recalled product is the GE LOGIQ E9 ultrasound system. It was sold to healthcare providers for medical imaging purposes and has a unique serial number assigned to each unit.
Immediately stop using the GE LOGIQ E9 ultrasound system as the power cord can break and expose electrical conductors, creating a shock hazard.
No, the GE LOGIQ E9 ultrasound system is intended for use by qualified physicians in medical settings, not home users.
Check if your unit has a serial number assigned, as each consignee (healthcare provider) receives one unique serial number for the GE LOGIQ E9 ultrasound system.
Immediately stop using the device and contact GE Medical Systems for further instructions.
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-2983-2018 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2983-2018 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.
