ClearanceBrief
Recall Z-0844-2018 ยท OWB Interventional Fluoroscopic X-Ray System

Toshiba American Medical Systems Inc

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

DateDec 29, 2017
StatusTerminated
ReasonDuring 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.
Root causeProcess control
ActionA 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 s
Quantity29 units
DistributionUnited States
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K133535INFX-8000V, V5.30
Toshibamedical Systems Corporation, Jul 23, 2014
K170909Infinix INFX-8000V, V6.40
Toshiba Medical Systems Coroporation, Jun 16, 2017