Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Philips Healthcare Brilliance 64 Computed Tomography X-Ray System Recalled by Philips Healthcare Due to Software Defects resulting in: (1) sagittal result shortened...

Date: September 6, 2015
Company: Philips Healthcare
Status: Terminated
Source: FDA (Device)

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 Brilliance 64 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

Affected (29 states)Not affected

About Philips Healthcare

Philips Healthcare has 21 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report