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# Philips BrightView CT System Recalled
- URL: https://www.fdaweb.com/philips-brightview-ct-system-recalled/
- Published: 2024-02-08T12:00:00.000Z
- Updated: 2026-09-14T14:22:30.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156323

Philips North America has recalled (Class 1) its BrightView computed tomography gamma camera system because of the risk of the detector unexpectedly falling due to a component failure. “If the detector is positioned below center of the gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation,” a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=205398&ref=fdaweb.com) says. “If the detector is positioned above center of the gantry, there may be an interruption to normal system operation.”