Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System Recalled by Philips Healthcare Due to Software Defects resulting in: (1) sagittal result shortened...
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 Healthcare directly.
Affected Products
Philips Healthcare Ingenuity Core128 Computed Tomography X-Ray System
Quantity: US - 423
Why Was This Recalled?
Software Defects resulting in: (1) sagittal result shortened for axial scans; (2) single series displayed on console viewer when Creating multi-planner reconstruction; (3) scan length changes with a change in field of view; (4) DoseRight algorithm miscalculations leading to incorrect CTDI values; (5) scan length changes during subsequent axial results, (6) surview scan lengths near 135mm or 184mm
Where Was This Sold?
This product was distributed to 29 states: AL, AZ, AR, CA, CO, FL, GA, IL, IN, IA, LA, MD, MA, MN, MS, MO, NV, NY, NC, OH, OK, OR, PA, SC, TX, VT, VA, WA, DC
About Philips Healthcare
Philips Healthcare has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report