GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-0606-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Discovery NM/CT 670 DR, model 5376204-70-56 intended for use in detecting, localizing, diagnosing of diseases and organ function for the evaluation of diseases, trauma, abnormalities, and disorders such as, but not limited to, cardiovascular disease, neurological disorders and cancer.

Product Classification:

Class II

Date Initiated: May 24, 2018

Date Posted: December 19, 2018

Recall Number: Z-0606-2019

Event ID: 81680

Reason for Recall:

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.

Status: Completed

Product Quantity: 4 units

Code Information:

GTIN 00840682124393 Serial Numbers: DDRW34032, DDRX34038, DDRX34041, DDRX34045

Distribution Pattern:

CA, DC, OH, UT, WI, Canada

Voluntary or Mandated:

Voluntary: Firm initiated