FDA Recall Terminated

INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM

Recall: Z-0844-2018 · Initiated December 29, 2017

Recall

Recall Number
Z-0844-2018
Event Number
79153
Firm
Toshiba American Medical Systems Inc
FEI Number
2020563
Product Code
OWB
Status
Terminated
Root Cause
Process control
Initiated
December 29, 2017
Terminated
November 29, 2023
Address
2441 Michelle Dr PO Box 2068, Tustin, CA, 92780-7047

Description

INFX-8000V Fluoroscopic X-Ray Systems; INFINIX CF-I/BP PLUS CARDIAC SYSTEM

Reason

During an examination a device error occurred and the ceiling drive operation was disabled. It was found that the fastening bolts of the driving portion of the ceiling drive loosened cause the error.

Action

A recall notification letter was sent to affected consignees on 12/29/2017. The following information was included in the notification letter: Should this problem occur prior to the above corrective action and in the middle of a clinical case, you will be able continue the case tentatively. The x-ray emissions will be still available and the inhibited ceiling support device can be overridden by pressing the override switch on the left side of the operation console. If any abnormalities are found during use, please stop using your system and contact your Toshiba service representative. Please share this information with all users and reviewing radiologist as well as clinical engineering and the biomedical group at your facility.

Distribution

United States

Quantity

29 units