FDA Device recall Z-0706-2017
Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provi…
- FDA Device
- Class II
- terminated
- Published 2016-12-14
On 2016-12-14 the FDA classified a Class II recall of Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provi… by Philips Medical Systems Cleveland, citing A software defect is causing issues with the IQon Spectral CT and Philips Spectral CT Applications while filming, saving and annotating images.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0706-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-14 |
| Published | 2016-12-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Medical Systems Cleveland |
| Distribution | AR, IN, LA, MA, MN, OR, TN |
Product
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.
Reason
A software defect is causing issues with the IQon Spectral CT and Philips Spectral CT Applications while filming, saving and annotating images
Identifiers
| code_info | 50001 50002 50004 50005 50006 50008 50009 50100 50101 50102 50103 430000 430001 430002 430003 430004 430006 430007 430501 430502 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0706-2017%22
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