GE Healthcare recalls Discovery NM/CT 670 Pro model 5376204-70-54 due to potential electric hazard from improper wiring of safety switches. 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 the Discovery NM/CT 670 Pro model 5376204-70-54 because safety switches might not shut off power correctly, creating an electric hazard. This could lead to electric shock or injury if the system is used without proper wiring.
The main disconnect switch, EPO button on the A1 panel, and Remote EPO buttons may not be wired correctly during installation. This means they might not shut off all power to the system as intended, potentially causing electric shock or injury.
Medical facilities using the Discovery NM/CT 670 Pro model 5376204-70-54 are most at risk. Patients and staff could face electric shock if the safety switches fail to shut off power.
Check for the model number 5376204-70-54 on the Discovery NM/CT 670 Pro system. The serial number starts with ESDX35015. This product was sold with GTIN 00840682121194.
Verify that the main disconnect switch, EPO button on the A1 panel, and Remote EPO buttons are wired correctly according to the manufacturer's instructions.
The recall indicates potential safety issues with wiring, so it is not safe to use without confirming correct wiring.
Check for the model number 5376204-70-54 and serial number starting with ESDX35015 on your Discovery NM/CT 670 Pro system.
Ensure the safety switches are wired correctly; contact GE Healthcare for further guidance if you suspect improper wiring.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0608-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0608-2019 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.
