Every recall we track for PHILIPS MEDICAL SYSTEMS — 11 in all — plus the complaints and injury reports the public filed about them.
Philips recalls certain Ingenuity CT scanners that may require manual triggering after Bolus Tracking scans, risking inadequate imaging and extra radiation exposure. Affected units include specific models sold in China and Brazil.
Philips recalls certain CT scanners that may require manual triggering after Bolus Tracking scans, risking inadequate imaging and extra radiation exposure. Affected units may need rescan.
Philips recalls IQon Spectral CT upgrades due to potential inadequate scans and extra radiation exposure from manual triggering after Bolus Tracking scans.
Philips recalls Spectral CT on Rails model 728334 with software issues that may cause gantry to stay at scan position after pressing Go. Affected units have specific serial numbers and software versions.
Philips recalls specific Incisive CT models with software versions 5.1.0.X and 5.1.1.X due to potential incorrect scans, patient rescans, and image quality issues. Affected units may require software updates to prevent safety risks.
Philips recalls CT 5300 scanners with specific software versions due to risks of incorrect scans, missing ECG data, and radiation errors. Affected units may need re-scanning or rescan due to software faults.
Philips Medical Systems recalls Incisive CT software versions 5.1.0.X and 5.1.1.X for Brazil SKD models. Issues may cause incorrect scans, rescans, or missing ECG data. Affected units must be updated by software fix.
Philips recalls Spectral CT on Rails with software version 5.1.0.X (model 728334) due to potential misdiagnosis from incorrect image labeling. Affected units may require software update to prevent incorrect treatment.
Philips recalls Spectral CT 7500 models with software version 5.0 due to potential misdiagnosis from incorrect image labeling. Affected units may require software update to prevent incorrect treatment.
Philips recalls CombiDiagnost R90 1.0 (709030) models due to potential display of previous patient radiography images during fluoroscopy exams, causing image content differences.
Philips recalls CombiDiagnost R90 1.1 (709031) models where RF viewer may display previous patient radiography images during fluoroscopy, causing image differences. Affected units have specific serial numbers.
