Brightview System
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Brightview Gamma Camera Sy. W/ 3/4" Crystal & Detector Caudal And Cephalic Tilt |
Not applicable. |
2170-3003A |
Brightview Gamma Camera Sy. W/ 3/8" Crystal & Detector Caudal Cephalic Tilt |
Not applicable. |
2170-3002A |
Brightview Gamma Camera System With 3/8" Crystal |
Not applicable. |
2170-3000A |
Brightview Gamma Camera System With 3/4" Crystal |
Not applicable. |
2170-3001A |
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
Additional information
Details
Philips Medical Systems Nederland B.V.
Veenpluis 6, Best, Netherlands, 5684 PC
Get notified
Receive notifications for new and updated recalls and alerts by category.