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