GE Healthcare, LLC: Medical Device Recall in 2018 - (Recall #: Z-2579-2018)

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 Digital Ready

Product Classification:

Class II

Date Initiated: May 24, 2018

Date Posted: August 8, 2018

Recall Number: Z-2579-2018

Event ID: 80484

Reason for Recall:

DIGITAL ReadyCT/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 5986030. a. Serial Number PTDMI1800003PT, System ID Number RADNETPT1839, UDI Number 01008406821209751118010421PTDMI1800003PT; b. Serial Number PTDMI1800005PT, System ID Number RADNETPT1838, UDI Number 01008406821209751118010421PTDMI1800003PT; c. Serial Number PTDMI1800009PT, System ID Number 813745DMIDR2, UDI Number 01008406821209751118021921PTDMI1800009PT

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