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.

776–796 of 796

  • ModerateFDA (Devices)·Z-1038-2013·2013-04-10

    Siemens COHERENCE RT Therapist Software Recall for Performance Defects

    Siemens Medical Solutions is recalling COHERENCE RT Therapist software versions to address performance defects and non-critical safety issues identified during final system testing.

    Product
    SIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B; Software release for COHERENCE Therapist 2.3 for Primus and Oncor Linear Accelerators; Model: COHERENCE Impression TH, Part No. 7341410, Current R630; Product Usage: The intend
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1037-2013·2013-04-10

    Siemens COHERENCE RT Therapist Software Recall for Safety Defects

    Siemens is recalling COHERENCE RT Therapist software versions for Primus and Oncor linear accelerators to address performance defects and safety issues.

    Product
    SIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B; Software release for COHERENCE Therapist 2.3 for Primus and Oncor Linear Accelerators; Model: COHERENCE TH, Part No. 7339125, - Current R630; Product Usage: The intended use of
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1039-2013·2013-04-10

    Siemens COHERENCE RT Therapist Software Recalled for Performance Defects

    Siemens Medical Solutions is recalling COHERENCE RT Therapist software versions due to performance defects and non-critical safety issues.

    Product
    SIEMENS brand COHERENCE RT Therapist versions RTT MR1.5, RTT 2.1/2.1A and RTT 2.2/ 2.2B; Software release for COHERENCE Therapist 2.3 for Primus and Oncor Linear Accelerators; Model: COHERENCE TH 2.0, Part No. 8139839, Current R630; Product Usage: The intended us
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0992-2013·2013-04-03

    Siemens Axiom Artis zeego Angiographic X-Ray System Recall

    Siemens is recalling 52 Axiom Artis zeego systems due to a potential risk to patients or operators during operation.

    Product
    Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical configuration Angiographic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0997-2013·2013-04-03

    Siemens Artis Angiographic X-Ray Systems Recalled for Image Registration Issues

    Siemens is recalling 81 Artis angiographic x-ray systems because a software issue may cause imprecise image registration during specific procedures.

    Product
    Artis Systems with Software Artis VC20x/VC21A/VD10x that have a DSA license installed. Angiographic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0930-2013·2013-03-20

    Siemens ACUSON S2000 ABVS Scanner Recalled for Sharp Transducer Edges

    Siemens is recalling 214 ACUSON S2000 ABVS systems because the transducer pod may contain sharp edges that could cause injury.

    Product
    ACUSON S2000 Automated Breast Volume Scanner (ABVS); Model number 10042541 Distributed by Siemens Medical Solutions USA Inc. business Unit: Ultrasound. The S2000 Automated Breast Volume Scanner (ABVS) Ultrasound System for imaging of the breast allows volumetric acquisitio
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0948-2013·2013-03-20

    Siemens CT Software Recall for Sporadic 3D Reconstruction Hang-Ups

    Siemens Medical Solutions is recalling 896 Somatom CT systems due to sporadic software malfunctions that cause 3D reconstructions to hang during preview.

    Product
    Siemens Somatom CTs equipped with software syngo CT2010A, syngo CT2010B, syngo CT2011A and CT2012B. Computed tomography x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0907-2013·2013-03-13

    Siemens ARTISTE syngo RT Therapist software recall for beam delivery error

    Siemens is recalling 5 ARTISTE digital linear accelerators due to a software defect that may cause repeated delivery of radiation beams.

    Product
    SIEMENS brand ARTISTE syngo RT Therapist (RTT) version 4.3, ARTISTE Model, Part No. 08162815, Digital linear accelerators, MOSAIQ OIS system, Distributed by SIEMENS Healthcare IM CR RO, CR Radiation Oncology, Manufactured by SIEMENS AG, MEDICAL SOLUTIONS, GERMANY.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0515-2013·2012-12-19

    Siemens MAVIG PORTEGRA 2 Surgical Light Recall for Missing Component

    Siemens is recalling 1,315 MAVIG PORTEGRA 2 surgical lights because a specific component may have been omitted during installation.

    Product
    MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0465-2013·2012-12-12

    Siemens syngo.plaza Radiological Image Processing System Software Update Recall

    Siemens Medical Solutions USA, Inc. is recalling 15 syngo.plaza systems to address unintended software behavior that may affect system performance.

    Product
    Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0480-2013·2012-12-12

    Siemens Mobilette Mira Mobile X-ray System Recalled for Image Loss Risk

    Siemens Medical Solutions USA is recalling 21 Mobilette Mira mobile x-ray systems due to a risk of lost images during examination.

    Product
    Siemens Mobilette Mira, intended use as Mobile x-ray system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0048-2013·2012-10-17

    Siemens syngo.plaza Radiological Image Processing System Recall

    Siemens is recalling 11 syngo.plaza systems due to a software defect where archived studies may be missing from the database.

    Product
    Siemens syngo.plaza radiological image processing system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2464-2012·2012-10-03

    Siemens MRI Systems Recalled for Potential Coil Heating During Imaging

    Siemens is recalling 370 MRI systems because the Flex Large 4 Coil can heat up in the electronic housing when positioned off-center.

    Product
    Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2367-2012·2012-09-19

    Siemens Mobilett Mira Mobile X-Ray System Recalled for Wheel Defect

    Siemens is recalling nine Mobilett Mira mobile x-ray systems because a loose center screw on the driving wheel may cause the system to become immobilized.

    Product
    Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2322-2012·2012-09-12

    Siemens Recalls Mobilett Mira Mobile X-Ray Systems Due to Switch Defect

    Siemens is recalling 20 Mobilett Mira mobile X-ray systems because a switch may become trapped, causing the unit to move continuously.

    Product
    Siemens Mobilett Mira. Mobile X-Ray System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2275-2012·2012-09-05

    Siemens syngo.plaza Radiological Image Processing System Recalled for Miscalculation

    Siemens Medical Solutions is recalling 14 syngo.plaza systems due to a potential miscalculation in images with pixel depth values greater than 12 bits.

    Product
    syngo.plaza, Model number 10592457. Intended use: radiological image processing system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2264-2012·2012-09-05

    Siemens syngo Imaging XS Software Recall for Miscalculation Defect

    Siemens Medical Solutions is recalling 52 syngo Imaging XS systems due to potential miscalculation of grey scale values in specific image processing functions.

    Product
    syngo Imaging XS. Radiological image processing system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2073-2012·2012-08-01

    Siemens Linear Accelerators Recalled for Potential Radiation Dosing Error

    Siemens is recalling 18 ARTISTE and ONCOR linear accelerators due to a rare software issue that could cause radiation beams to be delivered twice.

    Product
    ARTISTE or ONCOR Digital Linear Accelerators with syngo RT Therapist version 4.2/MOSAIQ OIS Systems and Multiple-X, Manufactured by SIEMENS AG. The ARTISTE and ONCOR family of Linear Accelerators are used to deliver X-ray photon and electron radiation for the therapeutic treatme
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2078-2012·2012-08-01

    Siemens syngo.plaza Radiological Image Processing System Recalled for Malfunction

    Siemens is recalling two syngo.plaza radiological image processing systems due to a potential malfunction where images may fail to load without an error message.

    Product
    Siemens syngo.plaza. Radiological image processing system
    Category
    Medical Device
    Distribution
    Distributed nationwide