GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-2580-2018)

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 MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring

Product Classification:

Class II

Date Initiated: May 24, 2018

Date Posted: August 8, 2018

Recall Number: Z-2580-2018

Event ID: 80484

Reason for Recall:

Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).

Status: Terminated

Product Quantity: 42 units total

Code Information:

Model Number 5454001-170. Serial Number (System ID Number): CJRPX1800016CN ( 4550966PT11), CJRPX1800017CN (561422MI), CJRPX1800018CN (617726PET1EB), CJRPX1800021CN (404616DMI)

Distribution Pattern:

Nationwide distribution to AL, CA, CO, FL, IL, IN, MA, MD, MI, MS, NC, NJ, NY,OH, OK, SC, TN, TX, VA.

Voluntary or Mandated:

Voluntary: Firm initiated