FDA recall Z-2800-2020

Shanghai United Imaging Healthcare Co., Ltd. · Class II · device

Product

uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and disorders in, but not limit to, oncology, cardiology and neurology.

Reason for recall

1) Service function problem may cause false marking of a bad channel resulting in ring artifacts; 2) Potential intermittent scout scanning interruption due to angle signal drift caused by external interference; 3) Metal edge overlap of mylar strip in gantry may create sharp edge. May lead to repeat scanning and abrasions (N/A for Serial No. 200036)

Distribution

US Nationwide distribution including in the state of Texas.

Key facts

Status
Terminated
Initiation date
2020-07-16
Report date
2020-08-19
Termination date
2022-07-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Shanghai, N/A, China

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2800-2020