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Siemens Medical Solutions USA Recalls
796 recalls on record · August 1, 2012 to July 8, 2026 · Medical Devices
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
March 20, 2013Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Somatom CTs equipped with software syngo CT2010A, syngo CT2010B, syngo CT2011A and CT2012B. Computed tomogra
Hazard: Sporadic hang-up malfunctions concerning 3D reconstructions during activated "Preview Image" functionality.
March 20, 2013Medical DevicesFDA
Siemens Medical Solutions USA, Inc. recalls ACUSON S2000 Automated Breast Volume Scanner (ABVS); Model number 10042541 Distributed by Siemens Medical Solutions U
Hazard: On some ACUSON S2000 ABVS systems, the inside of the transducer pod may contain sharp edges.
March 13, 2013Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls SIEMENS brand ARTISTE syngo RT Therapist (RTT) version 4.3, ARTISTE Model, Part No. 08162815, Digital linear accelerator
Hazard: Siemens became aware of a potential safety issue when using the "In-session resumption" feature of the syngo RT Therapist (RTT) 4.3 software. The RTT will send again the previously completed beam or segment for delivery to the control console, thus repeating the already delivered Monitor Units of the same beam or segment.
December 19, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Hazard: A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
December 12, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Mobilette Mira, intended use as Mobile x-ray system.
Hazard: There is a risk of lost images during examination.
December 12, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens syngo.plaza Radiological Image Processing System Usage: Radiological Image Processing System
Hazard: Firm has become aware of an unintended behavior when using syngo.plaza and issued an Update Instruction. The Update Instruction SY050/12/S provides a software update and addresses the following issues: - Patient Rename messages for the same patient are being continually processed for several days. This fills up the 'pcvdbsrv' log and potentially affects performance of the system. - Data could
October 17, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens syngo.plaza radiological image processing system.
Hazard: Siemens became aware of an unintended behavior when using syngo.plaza. In syngo.plaza within the online "Short Time Storage" (STS), some studies are marked with an archived icon, however, the entry in the Archive Database referring to the physical file may be missing.
October 3, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Ima
Hazard: When positioning the Flex Large 4 Coil (part No. 8625761) off-center in left-right direction as it is used for example for hip and shoulder imaging and, in addition at an off-center position with respect to the head-foot direction, the coil can heat up in the area of the electronic housing (white plastic lids).
September 19, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Mobilett Mira mobile x-ray system Product Usage: Mobile x-ray system
Hazard: During regular product monitoring, firm became aware of a potential issue with the Mobilett Mira system, (serial numbers 1034, 1038, 1041, 1042, 1043, 1050, 1053, and 1054. During normal clinical operation the center screw on the driving wheel may become loose resulting in system immobilization. There is no risk of the system tipping over or collapsing on the floor, however the system may tilt t
September 19, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Hazard: Siemens has discovered a possible hazard to patients or hospital personnel when tilting the Uroskop Access system starting with serial number 6076. When tilting the table on the Uroskop Access table, the motor may become disconnected and the entire table assembly may fall on the floor.
September 12, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens Mobilett Mira. Mobile X-Ray System.
Hazard: During regular product monitoring, Siemens has become aware of a potential issue with the Mobilett Mira system. During normal clinical operation the switch on the motor drive handle of the unit may become loose and slide horizontally to the right and become trapped under the cover. This may cause the system to continuously move. In response, Siemens has issued Update Instruction XP038/12/S to r
September 5, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls syngo.plaza, Model number 10592457. Intended use: radiological image processing system.
Hazard: There is a potential malfunction in which a miscalculation occurs for images with pixel depth values greater that 12 bit in certain functions.
September 5, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls syngo Imaging XS. Radiological image processing system.
Hazard: There is a potential malfunction when using syngo Imaging XS, version VA70A or higher. In some situations it can happen that a miscalculation is done for the grey scale values in the functions "Regions of Interest", "Pixel Lens", "Edge Enhancement" and "Histograms".
August 29, 2012Medical DevicesFDA
Siemens Medical Solutions, USA, Inc recalls syngo Dynamics Version 9.5
Hazard: If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's study.
August 1, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Siemens syngo.plaza. Radiological image processing system
Hazard: Siemens became aware of a potential malfunction when using syngo.plaza with software version VA20C_HF01. For datasets with distance measurements it can happen, that all images are not loaded to Viewer but no error message is displayed to user.
August 1, 2012Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls ARTISTE or ONCOR Digital Linear Accelerators with syngo RT Therapist version 4.2/MOSAIQ OIS Systems and Multiple-X, Manu
Hazard: Potential safety issue when using the IMMEDIATE RESUMPTION feature after a Control Console interlock during the delivery of flattening-filter-free (Multiple-X) beams or segments. In a very rare scenario, the RT Therapist will send again the previously completed beam or segment for delivery to the control console, thus repeating the already delivered Monitor Units of the same beam or segment.