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Official recall record

BrightView XCT Imaging System and Gamma Camera System

Health Canada — Medical Devices · 2024-01-05 · CanadaType I
Issuing authority
Health Canada — Medical Devices
Published
2024-01-05
Country of alert
Canada
Alert level
Type I
Alert type
recall

What the authority reported

Philips has become aware of a potential safety issue affecting BrightView systems where the detector may unexpectedly fall due to a component failure. A detector support component may fail due to unexpected wear: Scenario 1: If the detector is below the center of the gantry bore and the detector support component fails, the detector may descend downward unexpectedly and potentially contact the patient. Scenario 2: If the detector is above the center of the gantry bore and the detector support component fails, the detector will not be able to move to complete the imaging. Philips has received a complaint associated with this issue; however, there are no reports of injury or serious harm. Recall start date: December 20, 2023

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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