After CT image data from Toshiba is loaded, image mirroring can occur along the horizontal and vertical image axes. If this error occurs, the patient orientation/position may be…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
A video signal from one of the transceivers of the Large Display may be lost. In very rare cases, both transceivers of the Large Display could potentially fail which can lead to the loss of…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric shock if a person is in…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Siemens has become aware of three potential software issues with AXIOM Sensis or Sensis/ Sensis Lite systems. This may lead to a hazardous situation for patients if treatment cannot be…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
if the protective earth is interrupted and an additional fault leads to a fault current, the detection of the fault current may not be ensured may cause an electric shock if a person is in…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the…
Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.
Upgraded software version makes an automatic change in laser configuration settings for "markerless workflow" which may lead to the wrong laser offset coordinates being displayed in the…
Class IIFDA: TerminatedSiemens 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.
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.
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.
Software error may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
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.
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.
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.