Official recall record
BrightView XCT Imaging System and Gamma Camera System
- 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.
Record last checked against the registry on 2026-05-31.