Z-0018-2018 Class II Terminated

Recalled by Philips Electronics North America Corporation — Andover, MA

Recall Details

Product Type
Devices
Report Date
October 25, 2017
Initiation Date
January 18, 2017
Termination Date
February 26, 2020
Voluntary/Mandated
FDA Mandated
Product Quantity
US- 606

Product Description

Philips Healthcare Ingenuity Core128 X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.

Reason for Recall

During a bolus tracking procedure, no images were generated when the scan was completed, and the raw data file was not available for offline reconstruction. There is a discrepancy between the calculated reconstruction length and the actual scan length that results in the inability to reconstruct raw data. The operator may choose to rescan the patient.

Distribution Pattern

USA (nationwide) Distribution

Code Information

Software version 4.16