FDA Enforcement Class II Terminated

The Brilliance 64 and Ingenuity CT are whole body Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device may include signal analysis and display equipment, patient, and equipment supports, components and accessories.

Recall: Z-2223-2012 · Reported August 29, 2012

Enforcement

Recall Number
Z-2223-2012
Event ID
62641
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Philips Medical Systems (Cleveland) Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
N/A
Report Date
August 29, 2012
Initiation Date
July 18, 2012
Classification Date
August 17, 2012
Termination Date
February 22, 2013
Address
595 Miner Road, N/A, Cleveland, OH, 44143-2131, United States

Description

The Brilliance 64 and Ingenuity CT are whole body Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This device may include signal analysis and display equipment, patient, and equipment supports, components and accessories.

Reason

1. The current system design of software version 4.0.0xx379 does not prevent the system from scanning if the dose level exceeds a set upper dose limit for CT Brain Perfusion scanning, which previous versions did. However, the current version does have the Dose Check (NEMA XR-25) feature, which provides dose notifications and alerts, but it is possible for the user to disable Dose Check after ente

Code Info

System Code # 728231, Serial #s: 91003, 95157, 9654, 95130, and 95504 System Code # 728326, Serial #s: 300010, 300030, and 300018

Distribution

Worldwide Distribution - USA including IN and OH, also, the countries of Australia, Belgium, China, Israel, and Sweden

Quantity

8