Philips Medical Systems (Cleveland) Inc: Medical Device Recall in 2016 - (Recall #: Z-0706-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provide information about the chemical composition of the body materials and/or contrast agents.

Product Classification:

Class II

Date Initiated: November 14, 2016

Date Posted: December 14, 2016

Recall Number: Z-0706-2017

Event ID: 75755

Reason for Recall:

A software defect is causing issues with the IQon Spectral CT and Philips Spectral CT Applications while filming, saving and annotating images

Status: Terminated

Product Quantity: 20

Code Information:

50001 50002 50004 50005 50006 50008 50009 50100 50101 50102 50103 430000 430001 430002 430003 430004 430006 430007 430501 430502

Distribution Pattern:

Software was distributed in the following states: AR, IN, LA, MA, MN, OR and TN. Softward was also shipped to the following countries: Belgium, Denmark, France, Germany, Japan, Korea, Switzerland and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated