The Recall Desk
HighFDA (Devices)·Z-0608-2019·Announced 2018-12-19

GE Healthcare Discovery NM/CT 670 Pro Recalled for Electrical Wiring Defect

GE Healthcare is recalling one Discovery NM/CT 670 Pro unit because incorrect wiring may prevent emergency power shutoff, creating an electrical hazard.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a potential electric hazard (shock/fire risk) where injury has not yet been reported, fitting the 'High' severity criteria for risk-of-harm products without confirmed harm.

Plain-English summary

GE Healthcare, LLC is recalling one unit of the Discovery NM/CT 670 Pro, model 5376204-70-54. The recall was initiated because the Main disconnect switch, the EPO button on the A1 panel, and the Remote EPO button(s) may not have been wired correctly during installation.

This wiring defect could result in these controls failing to shut off all power to the entire system as intended, creating a potential electric hazard. The affected unit is identified by GTIN 00840682121194 and Serial Number ESDX35015.

The product was distributed in California, the District of Columbia, Ohio, Utah, Wisconsin, and Canada. Users of this specific medical device should contact GE Healthcare to verify the wiring configuration and address the potential safety issue.

The recalled product

Product
Discovery NM/CT 670 Pro, model 5376204-70-54
Manufacturer
GE Healthcare, LLC
Category
Medical Device — Imaging Equipment
Hazard
Affected units
1

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • GTIN 00840682121194 Serial Number ESDX35015

Distribution

Distributed in 5 states:

Part of a larger recall action

This product is one of 3 recalled by GE Healthcare, LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 3 products in this recall →

Related recalls

Same manufacturer · GE Healthcare, LLC

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Same hazard · electric shock

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