Every recall we track for Siemens Medical Solutions USA, Inc — 428 in all — plus the complaints and injury reports the public filed about them.
Siemens recalls ARTIS icono ceiling monitors (model 11328100) due to screws loosening over time, potentially causing the monitor to fall. Affected units may need repair or replacement.
Siemens recalls ARTIS icono ceiling model 11328100 due to potential loss of movement capability when adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
Siemens recalls ARTIS Icono Biplane model 11327600 due to potential loss of movement capability when adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
Siemens recalls ARTIS icono floor model 11327700 due to potential loss of movement capability after adjusting detector lift height to max or min limits. Affected units have specific serial numbers.
Siemens recalls ARTIS Pheno VE30A and VE40A models 10849000 for potential inaccurate 3D imaging that could lead to unintended low-dose radiation exposure during scans.
Siemens recalls ARTIS pheno and Icono biplane x-ray systems for potential sporadic dose increases during patient exams. Actual doses remain within regulatory limits but may cause unnecessary radiation exposure.
Siemens recalls ARTIS pheno model 10849000 interventional fluoroscopy systems that may show zero x-ray dose during patient exams, but actual radiation is still applied.
Siemens recalls ARTIS Icono biplane and ceiling models that may display 0 x-ray dose during patient exams, but actual radiation is still applied. Affected units have specific model numbers and UDI codes.
Siemens recalls LUMINOS Q.namix T X-ray systems with specific serial numbers due to potential display of previous patient images during single image acquisition. Affected units may need correction to prevent image overlap.
Siemens recalls specific LUMINOS Q.namix R X-ray systems with software version VB10D-SP02 due to potential display of previous patient images during single image acquisition. Affected units have unique serial numbers listed in the recall notice.
Siemens Medical Solutions recalls unapproved CT software applications that lack FDA 510(k) clearance. Affected users should contact Siemens for details on removal.
Siemens Medical Solutions recalls unapproved CT software applications that lack FDA 510(k) clearance. Affected users should check serial numbers listed in the official recall notice.
Siemens recalls unapproved CT software applications for SOMATOM X.ceed systems that lack FDA 510(k) clearance. Affected users should contact Siemens for details.
Siemens Medical Solutions recalls unapproved CT software applications that lack FDA 510(k) clearance. Affected users should stop using these applications until a fix is available.
Siemens recalls two ultrasound systems due to potential incorrect collimation when switching between organ programs. Affected models include LUMINOS Lotus Max (11574100) and Luminos dRF Max (10762471).
Siemens recalls MAMMOMAT Revelation breast imaging systems sold with bus-installation kits. These tables are designed for stationary use only and pose a risk if installed for bus applications.
Siemens recalls MAMMOM: Fusion models sold with bus-installation kits. These operator tables are designed for stationary use only and not safe for bus installations.
Siemens recalls MAMMOMAT Inspiration models sold with bus-installation kits. These operator tables are designed for stationary use only and not safe for bus installations.
Siemens recalls MAGNETOM Cima.X Upgrade model 11689304 due to potential ice blockage in helium venting system, risking helium leaks in MRI rooms.
Siemens recalls MAGNETOM Verio Dot MRI scanners with model 10684333 due to potential ice blockage causing helium leaks if a quench occurs. Affected units have specific UDI and serial numbers listed.
Siemens recalls BIOGRAPH One (DE) model 11689172 due to potential ice blockage in helium venting system, risking pressure buildup and helium leaks in MRI rooms.
Siemens recalls specific MAGNETOM Prisma MRI models (10849582) due to potential ice blockage in magnet venting system, which could cause helium pressure buildup and leak into scanning room.
Siemens recalls MAGNETOM Connectom.X model 11371480 due to potential ice blockage in helium venting system, which could cause pressure build-up and helium leaks during quenches.
Siemens recalls MAGNETOM Verio Dot Upgrade MRI machines with model 10684334 due to potential ice blockage in helium venting system, risking pressure build-up and helium leaks.
Siemens recalls specific MAGNETOM Cima.X (DE) MRI machines with model 11647158 due to potential ice blockage causing helium pressure build-up and system rupture.
Siemens recalls MAGNETOM Skyra fit MRI machines with model 10849580 due to potential ice blockage in helium venting system, risking pressure buildup and helium leaks during quench events.
Siemens recalls MAGNETOM Vida Fit MRI models with serial numbers 202010-202146. Ice blockage in venting system could cause helium pressure buildup and rupture, risking helium leaks in scanning rooms.
Siemens recalls MAGNETOM Vida (DE) MRI machines with model number 11060815 due to potential ice blockage in magnet venting system that could cause helium pressure build-up and rupture, leading to helium leaks in scanning rooms.
Siemens recalls MAGNETOM Skyra Fit BioMatrix MRI machines with model 11516217 due to potential ice blockage in helium venting system, risking helium leaks during quenches.
Siemens recalls MAGNETOM Spectra MRI units with model 10837643 and 10655588 due to potential ice blockage in magnet venting, risking helium system rupture and leaks in scanning rooms.
Siemens recalls MAGNETOM Lumina (DE) model 11344916 due to potential ice blockage in helium venting system that could cause pressure build-up and helium leaks during quench events.
Siemens recalls specific MAGNETOM Verio MRI models (serial numbers listed) due to potential ice blockage in helium venting system that could cause pressure build-up and helium leaks during quench events.
Siemens recalls Biograph mMR MRI machines with model 10433372 due to potential ice blockage in magnet venting, which could cause helium pressure buildup and system rupture.
Siemens recalls MAGNETOM Skyra MRI systems with model 10432915 due to potential ice blockage in helium venting system that could cause pressure build-up and helium leaks during quench events.
Siemens recalls Artis Pheno X-ray systems with model 10849000 due to limited movements after startup. Affected units have specific serial numbers. Contact Siemens for details.
Siemens recalls UROSKOP Omnia model 10094910 due to risk of overheating and fire from a faulty resistor. Affected units have specific serial numbers listed in the recall notice.
Siemens Medical recalls UROSKOP Omnia Max models with specific serial numbers due to resistor overheating that could ignite plastic housing. Affected units may need replacement.
Siemens recalls ARTIS angiography systems that may incorrectly report high radiation doses due to rare sensor-software communication failure. Affected systems require immediate attention to prevent potential overexposure risks.
Siemens Medical Solutions recalls interventional fluoroscopic x-ray systems due to rare risk of incorrect high dose reporting. Affected models include 4056869149325. No remedy specified in recall notice.
Siemens Medical recalls interventional fluoroscopic x-ray systems due to rare risk of incorrect high dose reporting. Affected models include 4056869295923. No remedy specified in recall notice.
Siemens Medical Solutions recalls interventional fluoroscopic x-ray systems that may incorrectly report high radiation doses due to rare sensor-software communication failure.
Siemens recalls ARTIS One Angiographic X-Ray Systems due to rare risk of higher radiation dose from incorrect copper prefiltration during x-ray releases. Affected units may require correction to prevent unintended radiation exposure.
Siemens recalls ACUSON Redwood 1.0 and 2.0 ultrasound systems with specific software versions that may convert liters to milliliters incorrectly, risking misdiagnosis. Affected units must be checked for software version and UDI.
Siemens recalls ACUSON Maple 1.0 diagnostic ultrasound systems with specific software versions due to potential misdiagnosis from incorrect unit conversions. Affected units may display 10x smaller values than actual, risking patient management errors.
Siemens recalls ACUSON Juniper 1.0-2.5 ultrasound systems with specific software versions due to potential misdiagnosis from incorrect unit conversions. Affected units may show values 10x smaller than actual liters.
Siemens recalls Sensis Vibe systems with software version VD15B due to potential crashes when adding certain reporting events. Affected units include specific serial numbers and models. Update to fix the issue.
Siemens recalls Sensis Vibe systems with VD15B software that may crash when adding certain reporting events. Affected units include specific model numbers for cardiac and interventional radiology procedures.
Siemens recalls Sensis Vibe systems with specific software version VD15B that may crash when adding certain reporting events. Affected units include specific serial numbers for cardiac and interventional radiology applications.
Siemens recalls Sensis Vibe systems with VD15B software that may crash when adding certain reporting events. Affected units have specific serial numbers and model numbers. No action is required but users should update software.
Siemens Medical recalls Multitom Rax X-ray systems where the support arm may unintentionally lower, causing injury during display positioning. Affected units have specific model numbers and may be identified through serial numbers.
Siemens recalls Luminos dRF Max displays with specific serial numbers due to risk of injury from support arm unintentionally lowering when positioned near people.
Siemens recalls Luminos Agile Max X-ray displays with risk of injury if support arm lowers unexpectedly during ceiling/wall suspension. Affected units have specific serial numbers.
Siemens recalls LUMINOS Lotus Max X-ray displays due to risk of injury if support arm lowers unexpectedly while positioning near ceiling/wall suspension.
Siemens recalls Vertix Solitaire touch displays due to short circuit risk in power supply causing overheating and fire. Affected units have specific serial numbers. Contact for return instructions.
Siemens recalls AXIOM MULTIX MT X-ray tables with short circuit risk in power supply causing fire. Affected models have specific serial numbers. Stop using immediately to prevent fire.
Siemens recalls AXIOM MULTIX MT X-ray tables due to short circuit in power supply causing fire risk. Affected models have specific serial numbers. Contact Siemens for remedy.
Siemens recalls AXIOM Vertix Solitaire devices due to fire risk from power supply overheating. Affected units have specific serial numbers; contact for return instructions.
Siemens recalls AXIOM MULTIX MP X-ray tables due to short circuit in power supply causing fire risk. Affected models have specific serial numbers. Contact Siemens for return or repair.
Siemens recalls Multix TOP I PRO X-ray tables with potential fire risk due to power supply short circuit. Affected units have specific serial numbers; contact Siemens for remedy.
Siemens recalls AXIOM MULTIX MP X-ray tables due to potential fire from power supply short circuits. Affected models include specific serial numbers; stop using immediately to prevent fire risk.
