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Siemens Medical Solutions USA Recalls
796 recalls on record · August 1, 2012 to July 8, 2026 · Medical Devices
Recalls by year
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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.
August 14, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to delive
Hazard: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zeego, Model Number 10280959
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee biplane MN, Model Number 10094143
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee floor MN, Model Number 10094142
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee biplane, Model Number 10094141
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee multi, Model Number 10094139
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee ceiling, Model Number 10094137
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Artis zee floor, Model Number 10094135
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dBC, Model Number 7728392
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis TC, Model Number 7728350
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dFC, Model Number 7727717
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dFA, Model Number 7555373
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dMP, Model Number 7555365
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dBA, Model Number 7555357
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dTC, Model Number 7413078
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dFC, Model Number 7412807
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dTA, Model Number 7008605
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis TA, Model Number 7007755
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis dBC, Model Number 5917054
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis BA, Model Number 5904656
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis BC, Model Number 5904649
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis MP, Model Number 5904466
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis FA, Model Number 5904441
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 31, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls AXIOM Artis FC, Model Number 5904433
Hazard: A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
July 17, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Cios care fusion system
Hazard: DAP chamber may be missing an insulating foil
July 17, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls Cios Alpha VA20/ VA30 mobile X-Ray systems
Hazard: DAP chamber may be missing an insulating foil
July 10, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Top, Model No. 11061648 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This c
Hazard: The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
July 10, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls SOMATOM go.All, Model No. 11061638 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This c
Hazard: The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
July 10, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Now, Model No. 11061618 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This c
Hazard: The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.
July 10, 2019Medical DevicesFDA
Siemens Medical Solutions USA, Inc recalls SOMATOM go.Up, Model No. 11061628 with syngo.CT software versions VA20A, VA20A_SP0, VA20_SP1. Product Usage: This co
Hazard: The potential sporadic performance problems may cause scanning workflow interruptions and unexpected user notifications resulting in diagnostic delay or need for patient rescan.