Z-0046-2017 Class II Terminated

Recalled by Toshiba American Medical Systems Inc — Tustin, CA

Recall Details

Product Type
Devices
Report Date
October 12, 2016
Initiation Date
April 25, 2016
Termination Date
July 13, 2017
Voluntary/Mandated
FDA Mandated
Product Quantity
165

Product Description

Toshiba America Medical Systems, Inc Aquilion Lightning TSX-035A CT Scanner.

Reason for Recall

It has been found that if the scan range extends beyond the maximum Field of View (FOV), a reconstruction operation error may occur. As a result, scanning may be interrupted and rebooting of the system may be necessary. Please note that this issue has not occurred in the U.S.

Distribution Pattern

US Distribution to the states of: PA, IA, MA, SD, MI, LA, KY, NC, NY, AR, IN, WI, OH, TY, FL, WV, WA, CT, MS, AL, ND, CO, HI, NO, MN, ID, OH, GA, MT, LA, NM, VT, TN, CA, NH, NJ, NE, SC and KS.

Code Information

LL 500