GE Healthcare recalls Discovery NM/CT 670 ES model 5376204-70-57 due to potential electric hazard from improper wiring during installation. Affected units may not shut off all power, risking electric shock.
When your system was installed, the Main disconnect switch, EPO button on the A1 panel, and Remote EPO button(s) (outside of the A1 panel) may not have been wired correctly which could result in these not shutting off all power to the entire system as intended, resulting in a potential electric hazard.
GE Healthcare is recalling certain Discovery NM/CT 670 ES MRI systems because improper wiring during installation could cause the system to not shut off all power, creating an electric hazard. This could lead to electric shock or other injuries if the system is used without proper safety features.
The main disconnect switch, emergency power-off button on the A1 panel, and remote EPO buttons may not have been wired correctly during installation. This means the system might not shut off all power as intended, potentially causing electric shock or other injuries.
Medical facilities using the specific model of Discovery NM/CT 670 ES MRI system with serial numbers ESDX35013 or ESDW35010 are affected. Staff and patients using these systems are at risk of electric shock if the system is not properly wired.
Check for the model number 5376204-70-57 on the Discovery NM/CT 670 ES system. Affected units have serial numbers ESDX35013 or ESDW35010. The product was sold with GTIN 00840682123877.
Verify that the main disconnect switch, A1 panel EPO button, and remote EPO buttons are wired correctly to ensure all power can be shut off.
The system may not shut off all power due to improper wiring during installation, creating an electric hazard that could cause electric shock.
Model 5376204-70-57 with serial numbers ESDX35013 or ESDW35010.
The recall does not specify a fix; users must check wiring to ensure all power can be shut off safely.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0607-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0607-2019 from GE Healthcare. 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.
