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 software errors are…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 system will display…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 system will display…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 system will display…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 acquisition of each…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Siemens Healthineers has identified a software error in previous software version VB10 for the Ysio fully automated system. The unit may process incorrect internal values for the position…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 system is unable to…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 misdiagnosis of a…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 x-ray possible,…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 x-ray possible,…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 x-ray possible,…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Software error which affects Sensis Vibe Hemo, Sensis and Sensis Vibe Combo systems with software version VD12A, which could cause possible hazard to patients, operators, or other persons…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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 isocenter which could…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 displayed, may result…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
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 the delay in…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Siemens Medical Solutions USA, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.