FDA Recall Terminated

Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System

Recall: Z-1719-2016 · Initiated September 6, 2015

Recall

Recall Number
Z-1719-2016
Event Number
74149
Firm
Philips Healthcare
FEI Number
1218950
Product Code
JAK
Status
Terminated
Root Cause
Radiation Control for Health and Safety Act
Initiated
September 6, 2015
Terminated
March 4, 2021
Address
3000 Minuteman Rd, Andover, MA, 01810-1032

Description

Philips Healthcare Ingenuity Elite Computed Tomography X-Ray System

Reason

Software Defects resulting in: (1) sagittal result shortened for axial scans; (2) single series displayed on console viewer when Creating multi-planner reconstruction; (3) scan length changes with a change in field of view; (4) DoseRight algorithm miscalculations leading to incorrect CTDI values; (5) scan length changes during subsequent axial results, (6) surview scan lengths near 135mm or 184mm

Action

Philips plans to initiate a field corrective action that will install a new software release to address the issue. Philips will modify the systems in the field to correct the defect at no cost to the customer. 1. You will contact customers and initiate a software update to correct the defect. 2. You will install the software and perform testing to ensure the software update was effective. 3. The customer notification letter which includes a statement that you will without charge, remedy the defect or bring the product into compliance. For further questions, please call (1-800) 722-9377, Option 5

Distribution

US Distribution - AZ, PA, FL, DC, W VA, NC, SC, AR, OK, OH, NY, NV, TX, PA, IN, CA, MN, MA, DC, MS, MD, OR, IL, CO, MO, VT, IA, AL, LA, GA and WA.

Quantity

US - 423