The Recall Desk

Manufacturer

Siemens Medical Solutions USA, Inc.

796 recalls in our database name Siemens Medical Solutions USA, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
796
Critical
16
Severe
69
Most recent
2026-07-08

Of the 796 recalls from Siemens Medical Solutions USA, Inc. we have scored against our rubric, 16 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 69 (9%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

601–625 of 796

  • HighFDA (Devices)·Z-0826-2016·2016-03-02

    Siemens Syngo Dynamics Software Recalled for Potential Patient Data Mixing

    Siemens is recalling Syngo Dynamics PACS software because it may mix data from multiple patients in echo trend graphs.

    Product
    software for Syngo Dynamics a Picture Archiving and Communication System (PACS) intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation. Syngo Dynamics is not intended to be used f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0862-2016·2016-03-02

    Siemens Recalls Syngo Plaza PACS Software Due to Display and Access Issues

    Siemens is recalling 68 units of Syngo Plaza PACS software to fix bugs affecting image display, saving, and access controls.

    Product
    Syngo Plaza Picture archiving and communication system. Software only. PACS intended to display, process, read, report, communicate, distribute, store and archive digital medical images. Stores and archives within DICOM structured reports. Integrates hospital/radiology informat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0687-2016·2016-01-27

    Siemens e.cam Gamma Camera Recall for Missing Operator Manuals

    Siemens is recalling 10 refurbished e.cam Dual Signature Gamma Camera systems because complete operator instruction manuals were not sent to customers.

    Product
    The e.cam Dual Signature Gamma Camera system. Used to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0597-2016·2016-01-13

    Siemens Syngo X-Workplace Software Recall for Incorrect Measurement Display

    Siemens is recalling Syngo X-Workplace software version VD10E because it may display incorrect length measurements, potentially leading to the selection of medical devices of the wrong size.

    Product
    Software version VD10E for Syngo X-Workplace; Picture archiving and communication system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0467-2016·2015-12-30

    Siemens MAGNETOM MRI Systems Recalled for Quench Line Installation Errors

    Siemens is recalling MAGNETOM MRI systems due to potential quench line installation errors that could cause oxygen displacement or cold burns.

    Product
    MAGNETOM systems, magnetic resonance diagnostic devices (MRDD).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0481-2016·2015-12-30

    Siemens Artis Fluoroscopic X-ray Systems Recalled for Display Soldering Defect

    Siemens is recalling 17 Artis fluoroscopic X-ray systems due to improper soldering in display modules that could cause video signal loss.

    Product
    Artis systems with large display from Siemens Medical Solutions USA, Inc. Interventional Fluoroscopic X-ray for angiographic procedures.
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0550-2016·2015-12-30

    Siemens Syngo Imaging XS PACS Recall for Incorrect Print Sizes

    Siemens is recalling 42 units of Syngo Imaging XS software because printouts may be in incorrect anatomical size when using unsupported printers.

    Product
    Syngo Imaging XS is a Picture Archiving and Communication System (PACS)
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-0319-2016·2015-12-02

    Siemens Syngo Imaging Software Recall for Version VB36D_HF02

    Siemens Medical Solutions is recalling three units of Syngo Imaging software to provide supplementary information regarding the release of Version VB36D_HF02.

    Product
    Syngo Imaging VB36D_HF02. Radiological image processing system.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0265-2016·2015-11-18

    Siemens Modularis VarioStar Lithotripter Recalled for Display Freeze Issue

    Siemens Medical Solutions is recalling 15 Modularis VarioStar lithotripters because a display freeze prevents current treatment data from being shown to users.

    Product
    MODULARIS VARIOSTAR; Lithotripter device designed to treat urolithiasis.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-0208-2016·2015-11-11

    Siemens e.cam Gamma Camera Recall for Radial Brake Failure

    Siemens Medical Solutions is recalling e.cam Gamma Camera systems due to a potential radial brake failure that could allow the detector to drift.

    Product
    e.cam Gamma Camera, an emission computed tomography system. It is intended to detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0168-2016·2015-11-04

    Siemens Medical Solutions Recalls 158 Radiation Therapy Machines

    Siemens Medical Solutions is recalling 158 radiation therapy machines due to a potential safety risk of the gantry colliding with patients or treatment tables.

    Product
    ONCOR Avant Garde, ONCOR Impression Plus, ONCOR Expression, ONCOR Impression, PRIMUS HI, MEVATRON M2/PRIMUS Mid-Energy, ARTISTE; intended use is to deliver x-ray radiation for therapeutic treatment of cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0118-2016·2015-11-04

    Siemens CIOS ALPHA Fluoroscopic X-Ray System Recalled for Potential Failure

    Siemens Medical Solutions is recalling 44 CIOS ALPHA fluoroscopic x-ray systems due to a potential system failure that could interrupt patient procedures.

    Product
    CIOS ALPHA; image intensified fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0182-2016·2015-11-04

    Siemens ACUSON SC2000 Ultrasound Systems Recalled for Hardware Defects

    Siemens is recalling 2,099 ACUSON SC2000 ultrasound systems due to hardware defects involving wheel lock disconnection and system lockups.

    Product
    ACUSON SC2000 ultrasound systems model 10433816 Imaging system that provides the ability to measure anatomical structures and calculation packages that provide info for clinical diagnosis purposes.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0107-2016·2015-10-14

    Siemens SOMATOM Force CT Systems Recalled for Software and Firmware Bugs

    Siemens Medical Solutions USA is recalling 21 SOMATOM Force computed tomography systems due to software and firmware bugs.

    Product
    SOMATOM Force; computed tomography x-ray system. Intended to generate and process cross-sectional images of patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0021-2016·2015-10-14

    Siemens SOMATOM Definition AS CT Scanner Software Recall

    Siemens Medical Solutions is recalling 113 SOMATOM Definition AS CT scanners to fix a software bug affecting visual warnings and image quality.

    Product
    SOMATOM Definition AS, intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0106-2016·2015-10-14

    Siemens Syngo RT Oncologist software update addresses safety issues

    Siemens Medical Solutions is updating Syngo RT Oncologist software versions 4.2 and 4.3 to fix safety and performance issues.

    Product
    Syngo RT Oncologist, an optional accessory to the linear accelerator system and permits localization, contouring, segmentation, image review, and review and approval of treatment plan parameters. In addition, it includes tools and administrative functions to aid in the diagnosis,
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0019-2016·2015-10-14

    Siemens SOMATOM Definition Edge CT Scanner Software Recall

    Siemens Medical Solutions is recalling 113 SOMATOM Definition Edge CT scanners due to a software bug affecting visual warnings and image quality.

    Product
    SOMATOM Definition Edge; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0020-2016·2015-10-14

    Siemens SOMATOM Definition Flash CT Scanner Software Recall

    Siemens Medical Solutions USA is recalling 113 SOMATOM Definition Flash CT scanners due to a software bug in version VA48A_SP0 that affects visual warnings and image quality.

    Product
    SOMATOM Definition Flash; intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2812-2015·2015-09-30

    Siemens Medical Solutions Recalls Linear Accelerator Systems Due to Collision Risk

    Siemens Medical Solutions is recalling 26 linear accelerator systems and associated software because a defect could cause automatic movement, posing a collision risk to patients.

    Product
    ARTISTE, ONCOR Avantgarde, ONCOR Impression Plus, ONCOR Expression, PRIMUS, PRIMUS Plus, Syngo RT Therapist; therapeutic treatment of cancer Product Usage: The intended use of the SIEMENS branded ARTISTE and ONCOR family of linear accelerator systems is to deliver X-Ray phot
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2783-2015·2015-09-23

    Siemens ACUSON SC2000 Ultrasound System Recalled for Data Capture Error

    Siemens is recalling ACUSON SC2000 ultrasound systems because a software error prevents the capture of images or clips when patient names are registered with different capitalization.

    Product
    ACUSON SC2000 Ultrasound System with software versions VB10B and lower; Model 10433816; Product Usage: The SC2000 ultrasound imaging system is intended for the following applications: Cardiac, Neo-natal and Fetal Cardiac, Pediatric, Transespohageal, Adult Cephalic, Peripheral
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2719-2015·2015-09-09

    Siemens Syngo.plaza PACS Recalled for Potential Data Loss and Mix-ups

    Siemens Medical Solutions is recalling 37 Syngo.plaza PACS units due to a potential issue that could lead to data loss and patient data mix-ups.

    Product
    Syngo.plaza; picture archiving and communications system Product Usage: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2437-2015·2015-08-26

    Siemens Intevo Series Imaging Systems Recalled for Overheating Risk

    Siemens Medical Solutions USA is recalling 185 Intevo Series imaging systems because improper fuses could cause the Power Controller assembly to overheat.

    Product
    Siemens Intevo Series system, a radiological imaging system that is a combination of a single photon emission computed tomography (SPECT) camera system for nuclear medicine images, and a computed tomography (CT) camera system for x-ray images.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-2436-2015·2015-08-26

    Siemens Symbia T Series Imaging Systems Recalled for Overheating Risk

    Siemens Medical Solutions is recalling Symbia T Series imaging systems because improper fuses could cause the Power Controller assembly to overheat.

    Product
    Siemens Symbia T Series, a radiological imaging system that is a combination of a single photon emission computed tomography (SPECT) camera system for nuclear medicine images, and a computed tomography (CT) camera system for x-ray images.
    Category
    Medical Device
    Distribution
    51 states
  • HighFDA (Devices)·Z-2435-2015·2015-08-26

    Siemens Symbia S Series Nuclear Medicine Imaging Systems Recalled for Overheating Risk

    Siemens is recalling Symbia S Series nuclear medicine imaging systems because improper fuses could cause the Power Controller assembly to overheat.

    Product
    Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine (NM) imaging system installed and used in only one location within an imaging facility or in a mobile/ transportable imaging environment.
    Category
    Medical Device
    Distribution
    51 states
  • ModerateFDA (Devices)·Z-2404-2015·2015-08-26

    Siemens Artis zee/zeego Systems Recalled for X-ray Locking Function Defect

    Siemens Medical Solutions is recalling 586 Artis zee/zeego angiography systems because a system error could prevent users from exiting the X-ray locking function without a restart.

    Product
    Artis zee/ zeego systems; dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide