GE Medical Systems recalls LOGIQ 9 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 9 ultrasound systems because the power cord can break, exposing electrical conductors and creating a risk of shock. This hazard affects medical devices used by qualified physicians for imaging procedures.
The power cord on the GE LOGIQ 9 ultrasound system can break, exposing electrical conductors inside. This creates a risk of electric shock if the device is handled improperly or comes into contact with water.
Healthcare providers who own or use the GE LOGIQ 9 ultrasound system for medical imaging are most at risk. The device is intended for use by qualified physicians in clinical settings.
The GE LOGIQ : 9 ultrasound system was sold to healthcare providers for medical imaging. Check the serial number on the device or the packaging for the specific model.
Inspect the power cord for any signs of damage or fraying before use.
Reach out to GE Medical Systems for guidance on next steps if the cord is damaged.
No, the GE LOGIQ 9 is intended for use by qualified physicians in medical settings only.
Check the serial number on the device or packaging to confirm it was sold to healthcare providers for medical imaging.
Inspect the power cord for damage and contact GE Medical Systems for further 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-2984-2018 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2984-2018 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.
