Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IQon Spectral CT with 4.7.2 software version.- Model 728332 Recalled by Philips Medical Systems (Cleveland) Inc Due to 23 Software related issues for the IQon Spectral...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems (Cleveland) Inc directly.
Affected Products
IQon Spectral CT with 4.7.2 software version.- Model 728332, a Philips Computed Tomography X-Ray System
Quantity: 63
Why Was This Recalled?
23 Software related issues for the IQon Spectral CT with 4.7.2 software version. These issues include: " Software errors that may result in CT spectral images misrepresentation or incorrect treatment; " Software errors that may result in partial set of images or inability to generate CT images.
Where Was This Sold?
Domestic and Foreign
About Philips Medical Systems (Cleveland) Inc
Philips Medical Systems (Cleveland) Inc has 313 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report