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Health Canada Medical devices

Brightview System

Issued December 22, 2023
Issue
Philips has become aware of a potential safety issue affecting Brightview systems that may present an extremity entrapment hazard to patients during a scan. While using pre-programmed motion (PPM) during an extrinsic quality assurance scan, a gap is created between the patient support and the detector. This gap presents a potential extremity entrapment hazard for patients while the system detectors and patient support are in motion. Recall Start Date: December 8, 2023
Hazard description
Performance
Product
Product name
Brightview System
Reference
ID
RA-74793