Every recall we track for Philips Medical Systems (Cleveland) Inc — 87 in all — plus the complaints and injury reports the public filed about them.
Philips recalls specific versions of its Pinnacle Radiation Therapy Planning System software due to a potential image error in head/feet orientations. Affected users should contact Philips for details.
Philips recalls Pinnacle 3 radiation therapy software version 18.0.5 due to potential incorrect stopping power ratio calculations. Affected units may require software update or correction.
Philips recalls specific Pinnacle3 radiation therapy software versions due to incorrect dose calculations when multiple beams are used, potentially affecting treatment accuracy.
Philips recalls Forte Gamma Camera Systems due to risk of detector falling unimpeded. Affected models include system codes 882290 and 882:1. No remedy specified in recall notice.
Philips recalls Forte Gamma Camera Systems due to potential detector falling unimpeded. Affected models include system codes 882320 and 882:1. No remedy specified in recall notice.
Philips recalls Forte Gamma Camera Systems due to potential detector falling unimpeded, which could cause injury. Affected units may need repair or replacement.
Philips recalls Forte Gamma Camera Systems due to risk of detector falling unimpeded, potentially causing injury. Affected units have specific system codes and serial numbers.
Philips Medical Systems recalls Forte Gamma Camera Systems due to potential detector falling. Affected units may require repair or replacement to prevent injury during medical imaging.
Philips recalls IQon Spectral CT Model #728332 x-ray systems with serial numbers 860004-860043, 860046-860127, 890002 due to potential image labeling errors during cardiac scans.
Philips recalls specific Vereos PET/CT systems (model 882446, serial 900004-900076) due to potential image labeling errors during cardiac scans. Affected units may require correction to prevent misdiagnosis.
Philips recalls specific models of Ingenuity Core CT scanners due to potential image labeling errors during cardiac step and shoot acquisitions. Affected units may produce incorrect phase tolerance labels in scans, requiring correction by medical professionals.
Philips recalls specific iCT SP computed tomography x-ray systems (model #728311) due to potential image labeling errors during cardiac scans. Affected units have unique serial numbers listed in the recall notice.
Philips recalls specific Ingenuity TF PET/CT models due to potential image labeling errors during cardiac scans. Affected units may show incorrect phase tolerance settings in certain cardiac imaging procedures.
Philips recalls specific Ingenuity CT x-ray systems (model 728326) due to potential cardiac imaging errors when phase tolerance settings are misconfigured during scans.
Philips Medical recalls specific iCT CT scanners due to potential image labeling errors during cardiac scans. Affected models may show incorrect phase tolerance settings in certain imaging procedures.
Philips recalls Brilliance 64 CT systems with specific serial numbers due to potential image labeling errors during cardiac step and shoot acquisitions, which could lead to incorrect phase tolerance application in scans.
Philips recalls specific models of Ingenuity Core128 CT scanners due to potential image labeling errors during cardiac scans. Affected units may show incorrect phase tolerance settings, requiring immediate action to prevent misdiagnosis.
Philips Medical recalls BrightView X model 882478 handcontrollers that may move unexpectedly after button release. Affected units have specific serial numbers. Stop using immediately to prevent unintended motion.
Philips recalls BrightView SPECT SPECT scanners with model 882480 that may cause uncommanded handcontroller movements. Affected units have specific serial numbers listed in the recall notice.
Philips recalls BrightView XCT model 882482 handcontrollers that may move unexpectedly after button release, posing a risk of unintended motion during medical procedures.
Philips Medical Systems recalls specific Vereos PET/CT models with misaligned front and rear covers that could create gaps or protrusions, potentially affecting imaging safety. Affected units have serial numbers starting with 900000.
Philips Medical recalls Ingenuity TF PET/CT (non-RoHS) model 882456 due to software issues. A safety update is required to prevent potential risks in medical imaging systems.
Philips Medical Systems recalls Brilliance 16 Slice CT scanners with model 728246 due to potential fiberglass resin separation that could cause gantry cover failure. Affected units have specific serial numbers listed in the recall notice.
Philips Medical Systems recalls specific Brilliance 10 Slice CT scanners where fiberglass resin separation could cause gantry cover failure, potentially leading to equipment malfunction.
Philips Medical Systems recalls Brilliance 64 CT scanners (Model 728231) due to potential fiberglass resin separation causing gantry front cover and support failure. Affected units have specific serial numbers listed in the recall notice.
Philips Medical recalls certain Brilliance 16 Slice CT scanners due to potential fiberglass resin separation causing gantry cover failure. Affected models include specific serial numbers listed in the recall notice.
Philips Medical recalls certain Brilliance 40 CT scanners (Model 728235) due to potential fiberglass resin separation causing gantry cover failure. Affected units have specific serial numbers listed in the recall.
Philips Medical Systems recalls Brilliance 6 Slice (Air) CT scanners with serial numbers starting from 365 to 3701 for potential fiberglass resin separation causing gantry cover failure.
Philips recalls specific Vereos PET/CT systems with software version 2.0.1 (model 882446) due to potential incorrect medical images causing misdiagnosis. Affected units have serial numbers from 900004 to 900067.
Philips recalls certain Brilliance 64 CT scanners that may produce ring or smudge artifacts on images due to a failing collimator compensator. Affected units were sold with specific serial numbers.
Philips recalls Brilliance iCT CT scanners that may produce ring or smudge artifacts on images due to collimator compensator failure. Affected units have exceeded expected usage lifespan.
Philips recalls certain Brilliance 16 Air CT scanners that may produce ring or smudge artifacts on images due to collimator compensator failure. Affected units were sold between 2018-2020.
Philips Medical recalls specific Ingenuity Digital PET/CT systems with model 882446 and serial numbers 900004-900035 due to potential misaligned screws in patient pallet connections.
Philips recalls specific Brilliance 64 CT scanners with DEPMED HARDENING KIT 12NC that may cause serious injury during patient motion. Affected units require immediate action to prevent permanent impairment.
Philips recalls specific Brilliance 16 P CT scanners with DEPMED HARDENING KIT 12NC model 728246 due to potential serious injury from patient support head holder contacting the back ISO shelter wall during motion.
Philips recalls Brilliance 16 CT scanners with specific serial numbers due to risk of serious injury from patient support head holder contacting the back wall during motion. Affected units require immediate action to prevent permanent impairment.
Philips recalls specific Ingenuity Core128/Elite models due to X-ray tube oil leakage risk. Affected units have serial numbers 336849-336855. Contact Philips for details.
Philips recalls specific Ingenuity TF PET/CT models with a defective X-ray tube that may leak oil, posing a risk to patients and users. Affected units have unique serial numbers and UDI codes.
Philips Medical recalls specific Ingenuity Core128 X-Ray Tube models with a production defect causing oil leakage. Affected units may pose patient or user risks if oil leaks occur.
Philips recalls specific models of Ingenuity Core X-Ray tubes with a production defect causing oil leakage. This could pose a risk for patients or users if the tube housing leaks oil. Affected units have unique serial numbers and UDI codes.
Philips recalls specific Brilliance Big Bore Radiology 728244 models due to potential oil leakage from X-ray tube housing, which could pose risks during use. Affected units have unique serial numbers and UDI codes.
Philips recalls Brilliance 64 CT scanners with specific software version due to failure to initialize low tube current scans. Affected units have serial numbers starting with 9134, 9667, etc. No action needed for safe use.
Philips recalls specific model Ingenuity TF PET/CT systems due to potential unresponsiveness after inactivity. Affected units may not complete scans. No remedy stated in recall notice.
Philips recalls specific models of Brilliance Big Bore CT scanners due to risk of couch movement during patient loading/unloading if Emergency Stop is closed.
Philips recalls Brilliance iCT SP CT scanners (model 728311) due to emergency stop button malfunction potentially causing couch movement during patient transfers. Affected units have specific serial numbers.
Philips recalls specific Brilliance 6 Slice CT scanners (model 728256) due to emergency stop button potentially disabling horizontal motion during patient transfers, risking injury.
Philips Medical Systems recalls Brilliance iCT CT scanners with serial numbers 100410-100814 and others. Closing the emergency stop may disable the horizontal motor, causing couch movement during patient load/unload. Affected units must be checked for serial numbers listed.
Philips recalls IQon Spectral CT scanners (model 728332) due to emergency stop button failure that may cause patient safety hazards during imaging procedures.
Philips recalls specific Brilliance 64 CT scanners (model 728231) due to emergency stop button malfunction that could cause patient movement during scans. Affected units have serial numbers 9541, 10207, 9890, 9633, 10561, 10655.
Philips recalls specific Ingenuity CT scanners (models 728325/728326) due to potential couch movement during patient loading/unloading if Emergency Stop is closed, which could cause injury.
Philips recalls certain Ingenuity Flex CT scanners where closing the emergency stop could allow the patient couch to move during patient loading or unloading, potentially causing injury.
Philips recalls certain Ingenuity Core 128 CT scanners (model 728323, 728324) due to risk of patient movement during scans if emergency stop is closed.
Philips recalls Brilliance 16 Slice CT scanners (model 728246) due to emergency stop button malfunction potentially causing patient safety risks during scans.
Philips Medical Systems recalls Ingenuity Core CT scanners with serial numbers 310204-333164. Closing the emergency stop may disable the horizontal motor, causing couch movement during patient loading/unloading. Affected units may need repair.
Philips recalls specific models of Brilliance Big Bore CT scanners due to risk of couch movement during patient loading/unloading if Emergency Stop is closed. Affected units have serial numbers listed in the recall notice.
Philips recalls IQon Spectral CT scanners with 4.7.2 software version due to potential misrepresentation of CT images or inability to generate images. Affected units have specific serial numbers.
Philips recalls specific Brilliance Big Bore CT scanners with 4.2.0 software that may cause image errors. Affected units include model 728244 with serial numbers listed. No remedy provided in official notice.
Philips recalls specific models of Brilliance Big Bore Oncology CT scanners due to software errors that may cause image generation failures or incorrect scans. Affected units have model # 728243 and serial numbers listed. No remedy is stated in the recall notice.
Philips recalls Precedence 16 Model 882350 imaging systems due to risk of collimator dropping during exchange, potentially causing injury to healthcare professionals.
Philips recalls BrightView X gamma cameras (model 882478) due to risk of collimator dropping during exchange, potentially causing injury. Affected units have specific serial numbers.
