FDA Recall Terminated

INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V series includes a floor mounted multi-axis positioner.

Recall: Z-1394-2015 · Initiated March 11, 2015

Recall

Recall Number
Z-1394-2015
Event Number
70748
Firm
Toshiba American Medical Systems Inc
FEI Number
2020563
Product Code
OWB
Status
Terminated
Root Cause
Device Design
Initiated
March 11, 2015
Posted
April 6, 2015
Terminated
September 18, 2015
Address
2441 Michelle Dr P.O. Box 2068, Tustin, CA, 92780-7047

Description

INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V series includes a floor mounted multi-axis positioner.

Reason

The table base rotational brake that holds the table top may not always be engaged when any force or side impact is applied to the table top.

Action

Toshiba sent a Urgent Medical Device Correction letter dated March 11, 2015, to all customers who purchased the CAT-880B catherization table for the Tosiba Infinix X-Ray Interventional System. The letter informed the customers of the problems identified and the actions to be taken. Customers were instructed to complete and return the attached form and fax it to (877) 349-3054 or email to [email protected]. Customers with questions were instructed to call (800) 421-1968 or contact their local Toshiba Representative at (800) 521-1968. For questions regarding this recall call 714-730-5000.

Distribution

Nationwide Distribution

Quantity

28 units