Philips Spectral CT Applications supports viewing and recall: Software Issue
Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provide…
Why was Philips Spectral CT Applications supports viewing and recalled?
A software defect is causing issues with the IQon Spectral CT and Philips Spectral CT Applications while filming, saving and annotating images
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
50001 50002 50004 50005 50006 50008 50009 50100 50101 50102 50103 430000 430001 430002 430003 430004 430006 430007 430501 430502
- Product
- Philips Spectral CT Applications supports viewing and analysis of images at energies selected from the available spectrum in order to provide…
- Recalling firm
- Philips Medical Systems (Cleveland) Inc
- Quantity
- 20
- Distribution
- 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.
- Recall date
- December 14, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)