FDA Enforcement Class II Terminated

Optima CT 520

Recall: Z-2585-2018 · Reported August 8, 2018

Enforcement

Recall Number
Z-2585-2018
Event ID
80484
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
GE Healthcare, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
August 8, 2018
Initiation Date
May 24, 2018
Classification Date
July 31, 2018
Termination Date
February 8, 2019
Address
3000 N Grandview Blvd, N/A, Waukesha, WI, 53188-1615, United States

Description

Optima CT 520

Reason

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).

Code Info

Serial number, CBCRG1700051HM, System ID Number 580622O520, UDI Number 01008406821025681117120021CBCRG1700051HM

Distribution

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

Quantity

42 units total