GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-2582-2018)

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:

Revolution CT 160 1.5D STD WAUK

Product Classification:

Class II

Date Initiated: May 24, 2018

Date Posted: August 8, 2018

Recall Number: Z-2582-2018

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 5590000-6. Serial number REVVX1800021CN (System ID 812842REV, UDI 01008406821185521118020021REVVX1800021CN), Serial Number REVVX1800004CN (System ID 269375REVOCT, UDI 01008406821185521118010021REVVX1800004CN).

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