Siemens Medical Solutions USA, Inc recalls
400 recalls in our records from 2012 to 2026: 400 FDA medical devices.
Recalls with full detail pages
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Siemens Medical Solutions USA, Inc medical device recall: MAGNETOM Cima.X Upgrade. Model Number: 11689304
There is a potential for an ice blockage to form or currently exist within the primary and/or the auxiliary venting paths of the magnet helium containment venting…
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Siemens Medical Solutions USA, Inc medical device recall: Biograph mMR. Model Number: 10433372
There is a potential for an ice blockage to form or currently exist within the magnet venting system. In the event of a quench, helium gas may be unable to escape…
Earlier and other recalls
These link to the official agency notice.
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS icono ceiling. Model Number: 11328100 Official notice ↗
Potential issue with the Display ceiling suspension (DCS Fix XL) that holds the monitor in place. Over time some screws that keep the monitor attached to the suspension…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS icono biplane. Model Number: 11327600 Official notice ↗
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno Official notice ↗
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS Pheno VE30A and VE40A Official notice ↗
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno and ARTIS Icono biplane Official notice ↗
During patient examinations, the system may sporadically display a major increase of the x-ray dose applied to the patient. Despite the reported dose showing…
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Siemens Medical Solutions USA, Inc medical device recall: SOMATOM X.ceed Software applications: syngo.CT Brain Quantification… Official notice ↗
To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.
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Siemens Medical Solutions USA, Inc medical device recall: Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R Official notice ↗
Ortho images acquired with preset automatic horizontal flip are not flipped and when acquiring single images, there is the possibility that an image of a previous…
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Siemens Medical Solutions USA, Inc medical device recall: LUMINOS Lotus Max Official notice ↗
A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling…
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Siemens Medical Solutions USA, Inc medical device recall: MAMMOMAT Revelation Official notice ↗
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as…
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Siemens Medical Solutions USA, Inc medical device recall: Artis Pheno. Image-Intensified Flouroscopic X-Ray System Official notice ↗
Limited system movements after startup .
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS is a family of dedicated angiography systems developed for… Official notice ↗
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system…
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Siemens Medical Solutions USA, Inc medical device recall: UROSKOP Omnia. Model Number: 10094910 Official notice ↗
A resistor in the frequency inverter may strongly overheat potentially igniting the plastic housing of the frequency inverter on fire.
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS One Angiographic X-Ray System Official notice ↗
A potential issue with ARTIS One systems was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect…
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON Juniper 1.0 Official notice ↗
If ultrasound systems with software, are changed from factory default to : 1) Milliliters per second (ml/sec, mL/sec) or 2) Milliliters per minute (ml/min, mL/min); then…
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Siemens Medical Solutions USA, Inc medical device recall: Luminos Agile Max -Intended to visualize anatomical structures by… Official notice ↗
The support arm may unintentionally lower resulting in injury to persons when they are under the display ceiling/wall suspension when positioning the displays
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Siemens Medical Solutions USA, Inc medical device recall: Sensis Vibe systems with software version VD15B in combination with… Official notice ↗
If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual),…
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Siemens Medical Solutions USA, Inc medical device recall: AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient… Official notice ↗
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON Juniper Diagnostic Ultrasound System Official notice ↗
On ultrasound systems, when Cardiac DICOM SR feature is configured to display either minimum or maximum measured value, and multiple cardiac region measurements are…
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Siemens Medical Solutions USA, Inc medical device recall: Siemens Artis Models: Interventional Fluoroscopic X-Ray… Official notice ↗
Coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the system…
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Siemens Medical Solutions USA, Inc medical device recall: Sensis Vibe Hemo Official notice ↗
The possibility of the Sensis documentation functionality application to crash.
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS icono Official notice ↗
Potential hardware issue for ARTIS icono ceiling system: collision sensor may falsely signal non-existing collisions for up to half an hour when the system is switched…
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Siemens Medical Solutions USA, Inc medical device recall: Mobilett Mira wireless Official notice ↗
Due to the incorrect mounting of the buzzer component, there is no acoustic signal during x ray activation. Otherwise, the system is fully functional, and x ray is…
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Siemens Medical Solutions USA, Inc medical device recall: Siemens Cios Alpha Official notice ↗
Software issue for Cios Alpha, Cios Flow, and Cios Spin VA30 systems, fulfillment of new requirements from DIN and IEC standards for Cios VA30 systems required may…
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Siemens Medical Solutions USA, Inc medical device recall: (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM… Official notice ↗
In some cases, when lubricating grease is present within the headband of the over-ear headphones, it may cause visible, dot- or lineshaped, fat-isointense artifacts…
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON Redwood 2.0 ultrasound systems Official notice ↗
If a user-generated preset for an 18L6 transducer created on a 1.0 ultrasound system is used with a 2.0 ultrasound system, the 2.0 ultrasound system will display…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS icono biplane -Angiography systems developed for single and… Official notice ↗
Due to a hardware issue in the cable connectors of the system generator, a thermal overload in the cable connections may occur when performing excessive…
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Siemens Medical Solutions USA, Inc. medical device recall: The following Pro.specta Emission Computed Tomography Systems that… Official notice ↗
During a whole-body planar scan with auto-contour, there is a possibility the short-linear drive (SLD) look-ahead sensors may trigger earlier than expected and may…
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Siemens Medical Solutions USA, Inc medical device recall: Cios Select VA 21 with FD- A Mobile X-ray system intended for use in… Official notice ↗
Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric…
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Siemens Medical Solutions USA, Inc medical device recall: Luminos Agile Max Official notice ↗
Under certain unlikely circumstances during a fluoroscopic examination, the imaging system Fluorospot Compact might sporadically display an incorrect air kerma/air kerma…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno systems with a Siemens Healthineers table or… Official notice ↗
If, during the procedure, X-ray has been released and a reference image has been stored, the following issue may occur: If "Adjust C-arm to Ref" is activated when the…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS one with a hybrid cable- An angiography system developed for… Official notice ↗
Examination room monitor connected with the hybrid cable may have a display issue and no image function is available
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno systems with a Siemens Healthineers table or a Trumpf/… Official notice ↗
In the event of any unintended table movement, the system may not detect the incorrect direction, could lead to the injury of a patient, staff member, operator, or…
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Siemens Medical Solutions USA, Inc medical device recall: Luminos Agile with software VC10 - A diagnostic imaging system for… Official notice ↗
Potential risk of collision with the ceiling, wall, or objects which may result in serious injury to staff or patients due to room configuration parameters of the system…
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Siemens Medical Solutions USA, Inc. medical device recall: SIEMENS Biograph Horizon 3R Mobile Official notice ↗
This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.
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Siemens Medical Solutions USA, Inc medical device recall: System Material # Artis zee floor 10094135 Artis zee ceiling 10094137… Official notice ↗
In rare cases, the system may only boot into backup mode after an abrupt shutdown and not reach full operating mode. This may result in a situation where it is necessary…
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Siemens Medical Solutions USA, Inc medical device recall: Software : myNeedle Guide 2D license Official notice ↗
In the syngo.CT VA40 and syngo.CT VA50 myNeedle Guide application, the order of the orientation labels head , center, and feet in the axial thick slice segments are…
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Siemens Medical Solutions USA, Inc medical device recall: AXIOM Luminos TF Official notice ↗
There is potential for the footrest to detach from the patient table during use.
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno Official notice ↗
Mechanical connection between the tabletop and table base may be lost.
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Siemens Medical Solutions USA, Inc medical device recall: Programmable Diagnostic Computer Official notice ↗
The firm will be performing a software update to address a software error which affects the listed products. This correction addresses four potential software issues: 1)…
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Siemens Medical Solutions USA, Inc medical device recall: Artiste Official notice ↗
When selecting the site fraction group for treatment, the User may select the wrong site for treatment, and potentially deliver the dose to wrong isocenter
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno Official notice ↗
Siemens has become aware of three potential software issues with ARTIS pheno systems with software version VE10B. This may lead to a hazardous situation for patients if…
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Siemens Medical Solutions USA, Inc medical device recall: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281… Official notice ↗
Siemens has become aware of a potential hardware issue with Artis Q, Artis Q.zen, Artis pheno and Artis icono systems with a specific lot of X-ray tubes. In rare cases,…
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Siemens Medical Solutions USA, Inc medical device recall: AXIOM Sensis or Sensis Vibe Combo systems as follows: System Material… Official notice ↗
The Sensis Signal Input Box provides hooks as a milled item on the bottom of the box support the possibility of mounting the Signal Input Box on an accessory rail (e.g.,…
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Siemens Medical Solutions USA, Inc medical device recall: Sensis with software version VD12A. A diagnostic and administrative… Official notice ↗
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zeego Official notice ↗
It may occur that after system startup no stand movement is possible any longer in the event of a discharged BIOS battery of the robotic stand control PC. If this…
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Siemens Medical Solutions USA, Inc medical device recall: Artis Icono Official notice ↗
During system tests, an increased wearing of the Image acquisition system fans has been observed. This could lead to an electrical failure which may cause malfunction of…
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Siemens Medical Solutions USA, Inc medical device recall: syngo Application software VE20 Official notice ↗
After CT image data from Toshiba is loaded, image mirroring can occur along the horizontal and vertical image axes. If this error occurs, the patient…
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Siemens Medical Solutions USA, Inc medical device recall: Artis Pheno Official notice ↗
A video signal from one of the transceivers of the Large Display may be lost. In very rare cases, both transceivers of the Large Display could potentially fail which can…
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Siemens Medical Solutions USA, Inc medical device recall: Artis icono biplane -angiography systems developed for single and… Official notice ↗
if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric…
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Siemens Medical Solutions USA, Inc medical device recall: Sensis Official notice ↗
Siemens has become aware of three potential software issues with AXIOM Sensis or Sensis/ Sensis Lite systems. This may lead to a hazardous situation for patients if…
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Siemens Medical Solutions USA, Inc medical device recall: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Model… Official notice ↗
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being…
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Siemens Medical Solutions USA, Inc. medical device recall: Acuson 9vE4 Transducer Official notice ↗
Transducers (component of ultrasound system) may exceed recommended thermal index limits
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Siemens Medical Solutions USA, Inc medical device recall: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM… Official notice ↗
Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may…
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Siemens Medical Solutions USA, Inc medical device recall: Artis icono biplane- in combination with a Siemens Healthineers table… Official notice ↗
Five potential software issues affecting Artis pheno and Artis icono systems in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). The potential…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee floor Official notice ↗
If the coolant level in the cooling circuit drops below a certain level, this may result in a situation in which the X-ray tube is no longer sufficiently cooled and the…
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Siemens Medical Solutions USA, Inc. medical device recall: Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems Official notice ↗
There is a quality issue with the three bolts that hold the CT balancing weights, which could create a safety issue.
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Siemens Medical Solutions USA, Inc medical device recall: YSIO X.Pree Official notice ↗
For the automated multi-image-acquisition procedure Ortho x-ray collimation is set in a preparative stage for the entire examination area prior to the exam. During…
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Siemens Medical Solutions USA, Inc medical device recall: Ysiosystem with VC10 software version Official notice ↗
Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal…
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Siemens Medical Solutions USA, Inc. medical device recall: Diagnostic Ultrasound System Official notice ↗
The clip store function in the ultrasound imaging system does not work when the system has a disk full error. This could cause a delay in treatment if the ultrasound…
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B Official notice ↗
Due to a calculation error in the measurement when using 2D trace (manual trace) tool. The trace circumference value is overestimated and may potentially result in…
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Siemens Medical Solutions USA, Inc medical device recall: Artis pheno with software VE20C- diagnostic imaging angiography… Official notice ↗
Four potential software issues with Artis pheno and Artis icono systems with software VE20C: 1. Updated calibration data not saved with measurement after scene+/-; 2. No…
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Siemens Medical Solutions USA, Inc medical device recall: 1. Sensis Official notice ↗
Software error which affects Sensis Vibe Hemo, Sensis and Sensis Vibe Combo systems with software version VD12A, which could cause possible hazard to patients,…
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Siemens Medical Solutions USA, Inc medical device recall: SOMATOM Confidence -Computed tomography systems Model 10590100 Official notice ↗
Software version VB20_SP5 my lead to a relevant degradation of head image quality, a potential risk to patients is misdiagnosis.
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Siemens Medical Solutions USA, Inc medical device recall: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver… Official notice ↗
Potential safety issue under specific preconditons that may result in a user selecting the wrong site for treatment with the possibility to deliver dose to the wrong…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee floor with software VD12-angiography systems developed for… Official notice ↗
If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is…
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Siemens Medical Solutions USA, Inc medical device recall: SOMATOM Force with software syngo.CT VB20 Model #10742326 Official notice ↗
software syngo.CT VB20 in the installed base, with or without syngo.CT software versions VB20_SP1, SP2, SP3, or SP4, may result in workflow interruptions resulting in…
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Siemens Medical Solutions USA, Inc medical device recall: Sensis/ Sensis Vibe systems with software VD1X as follows Official notice ↗
System operator manual states that the system should be rebooted once, every 7 days. In some cases, users are not following these instructions and the system is running…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zeego Official notice ↗
Software error, the software can produce an incorrect interpretation of the table rotation if the table has been rotated by more than 4degrees in either direction. This…
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Siemens Medical Solutions USA, Inc medical device recall: Computed tomography x-ray systems with software syngo.CT VA20A_SP4a Official notice ↗
Software versions may result in sporadic problems causing scanning workflow interruptions and unexpected user notifications. Sporadic software errors may also occur…
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Siemens Medical Solutions USA, Inc medical device recall: syngo.via RT Image Suite with syngo.via VB30 Official notice ↗
Potential for data loss when using the contouring or patient marking workflow when editing a structure set after saving and reopening a study, resulting in an incomplete…
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON Juniper Diagnostic Ultrasound System Official notice ↗
Due to intermittent failures of the power supply in the ultrasound system which renders it inoperable.
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Siemens Medical Solutions USA, Inc medical device recall: Artis Models with SW version VD12 listed below: Artis zee floor… Official notice ↗
Due to a software error, the IAS (Image Acquisition System) may sporadically fail during startup/ restart, and result in delay of clinical treatment
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS pheno- angiography systems developed for single and biplane… Official notice ↗
Software error VE10B -In case of a fault within the drivetrain of an axis and while performing a stepped peripheral imaging (PERISTEPPING/PERIVISION), the C-arm may…
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Siemens Medical Solutions USA, Inc medical device recall: Multitom RAX with software version VF10 Official notice ↗
Siemens identified two issues, In some cases, it is possible to perform an image acquisition although more than 20% of the beam does not hit the detector. This may only…
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Siemens Medical Solutions USA, Inc medical device recall: Artis systems - Product Usage: an angiography systems developed for… Official notice ↗
Due to inappropriate cleaning, some Artis systems show unexpected corrosion of visible belts which are needed to move system parts (e.g. C-Arm), Increased corrosion may…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model… Official notice ↗
Some Artis zee ceiling systems show an increased abrasion of the cabling at the cable outlet of the inner C-arm, the limited functionality may not be sufficient to…
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Siemens Medical Solutions USA, Inc medical device recall: Interventional Fluoroscopic X-Ray System ARTIS icono biplane-… Official notice ↗
Siemens has become aware of a potential issue with software version VE20C. Planned procedures may have to be terminated and performed on an alternative x-ray system.
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Siemens Medical Solutions USA, Inc medical device recall: Sensis/ Sensis Vibe Hemo systems with VD12A software as follows:… Official notice ↗
Due to the configuration of certain Windows Service Permissions within the operating systems of the Sensis/ Sensis Vibe computer, there is a risk for exposure of…
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Siemens Medical Solutions USA, Inc medical device recall: Ysio X.pree Official notice ↗
A patient image was assigned to a different patient during image recovery process. In the unlikely event of interrupted connection to a MAX detector during initiated…
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Siemens Medical Solutions USA, Inc. medical device recall: Product Label - ACUSON Sequoia *** Power Input: 100-240V~ Official notice ↗
The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational Sac Diameter (GSD) into the Estimated Date of Delivery (EDD) calculation. This may result in…
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Siemens Medical Solutions USA, Inc medical device recall: Interventional Fluoroscopic X-Ray System - Product Usage: developed… Official notice ↗
Siemens has become aware of a potential issue in which the imaging system UPS sporadically forces a shutdown of the imaging system PC without a true power supply problem.
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Siemens Medical Solutions USA, Inc medical device recall: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the… Official notice ↗
SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a, may result in sporadic problems causing scanning workflow interruptions and unexpected…
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Siemens Medical Solutions USA, Inc medical device recall: Sensis / Sensis Vibe systems with software version VD12 and equipped… Official notice ↗
System may sporadically freeze (lock-up) during operation or while being in an idle state, no longer possible to interact with the system
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model:… Official notice ↗
Misleading error messages and a gap in the Operator Manual which affects ARTIS Icono biplane or ARTIS Icono floor systems with software version VE20B. Potential issues…
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Siemens Medical Solutions USA, Inc medical device recall: SOMATOM Force Official notice ↗
System does not trigger a cancel command followed by a reload of the scan with the new parameter(s). This issue may result in a delay in diagnosis and/or need for…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee/ zeego & Artis Q/ Q.zen Artis Pheno Official notice ↗
When the user changes frame rates from lower frequency (e.g. 10 f/s) to higher frequency (e.g. 30 f/s) during continuous release of Fluoro "Fluoro Override", the…
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Siemens Medical Solutions USA, Inc medical device recall: Uroskop Omnia Official notice ↗
After the March 2019 corrective action on the monitor support arm, there is a residual risk of the support arm becoming dislodged in cases when the monitor support arm…
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee floor Official notice ↗
Some electronic components within the generator were equipped with an incorrect protection diode. As a result, protection against overvoltage may be inadequate, and the…
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Siemens Medical Solutions USA, Inc medical device recall: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:… Official notice ↗
There is a software problem which affects the DSA Roadmap application on ARTIS Icono and ARTIS Pheno systems with software version VE20B. In rare cases, when the DSA…
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Siemens Medical Solutions USA, Inc medical device recall: Siemens Artis one systems with a Display Port… Official notice ↗
Potential malfunction in which the examination room monitor may become intermittently dysfunctional (e.g., no display/flicking/wrong resolution).
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Siemens Medical Solutions USA, Inc medical device recall: Artis zee or Artis Q systems Official notice ↗
Potential exists for the collision supervision not to work properly following loss of the individual room configuration data settings causing danger of collision with…
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Siemens Medical Solutions USA, Inc. medical device recall: ACUSON AcuNav Volume Intracardiac Echocardiography Catheter 12.5F Official notice ↗
Due to adverse events received by the firm for left atrial perforations and Atrioventricular Node block.
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Siemens Medical Solutions USA, Inc medical device recall: Software versions syngo.CT VB20 or VB20_SP1 in the following systems:… Official notice ↗
Sporadic problems with the current software may result in scanning workflow interruptions and unexpected user notifications causing delay in diagnosis or patient rescan
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Siemens Medical Solutions USA, Inc medical device recall: Software: Syngo.via RT Image Suite software version VA30_SP02 with… Official notice ↗
Calibration offset between the central CT image plane and the external RT lasers has been set automatically to the factory default of 50.00 cm, if the misadjustment of…
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Siemens Medical Solutions USA, Inc. medical device recall: Symbia S-Series and Symbia T-Series - Product Usage: Intended use of… Official notice ↗
This letter is to inform you of the possibility that your Symbia S or Symbia T system(s) may have unintended slow motion of the detectors in specific situations which…
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Siemens Medical Solutions USA, Inc medical device recall: Siemens Sensis Vibe Hemo system in combination with the MicroPodTM… Official notice ↗
The connector linking the EtCO2 module to the HemoBox may break and become damaged, if the connector is re-attached to the HemoBox in this damaged state, under certain…
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Siemens Medical Solutions USA, Inc. medical device recall: E.cam or Symbia systems that use foresight detectors - Product Usage:… Official notice ↗
E. CAM and Symbia system with foresight detectors performing gated or dynamic acquisition may lose some detector time information. Our risk analysis indicates that the…
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Siemens Medical Solutions USA, Inc medical device recall: Cios Alpha Official notice ↗
Siemens has become aware of a hardware error which affects Cios Spin and Cios Alpha systems after the previous repair of the X-ray Generator with an integrated Energy…
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Siemens Medical Solutions USA, Inc medical device recall: Cios Alpha Official notice ↗
Hardware error- Hot Plugging feature could cause an electrical malfunction on the main control D80 (below revision 04 installed) of the generator which is part of the…
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Siemens Medical Solutions USA, Inc medical device recall: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage:… Official notice ↗
Two software issues (1) Using the override function in case of blocked system movements affecting Luminos dRF Max, Luminos Agile Max and Uroskop Omnia Max systems may…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.