GE Healthcare recalls Discovery NM/CT 670 DR model 5376204-70-56 due to potential electric hazard from incorrect wiring during installation. Affected units may not shut off all power, risking electric shock. Contact GE for remedy.
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 specific Discovery NM/CT 670 DR medical imaging systems because improper wiring during installation could cause electrical hazards. This means the system might not shut off all power properly, potentially causing electric shock to users.
The Main disconnect switch, EPO button on the A1 panel, and Remote EPO buttons may not have been wired correctly during installation. This could mean the system doesn't shut off all power as intended, creating a risk of electric shock if the system is turned on.
Healthcare facilities that installed the Discovery NM/CT 670 DR model 5376204-70-56 between 2019 and 2021 are affected. Medical staff and patients using these systems are at risk of electric shock if the wiring is incorrect.
Check for the model number 5376204-70-56 on the device. Serial numbers DDRW34032, DDRX34038, DDRX34041, and DDRX34045 are affected. These units were sold between 2019 and 2021.
Verify that the Main disconnect switch, EPO button on the A1 panel, and Remote EPO buttons are wired correctly.
The model number is 5376204-70-56.
The affected serial numbers are DDRW34032, DDRX34038, DDRX34041, and DDRX34045.
These units were sold between 2019 and 2021.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0606-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0606-2019 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.
