Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Discovery NM/CT 670 Pro Recalled by GE Healthcare, LLC Due to When your system was installed, the Main disconnect...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Healthcare, LLC directly.
Affected Products
Discovery NM/CT 670 Pro, model 5376204-70-54
Quantity: 1 unit
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 5 states: CA, OH, UT, WI, DC
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report