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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

37,779 Total Recalls

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 related to the block movements function and manual rotation of the flat detector. Depending on the status of the intervention, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where clinical treatment may be delayed until an additional restart is performed

Feb 25, 2022 Diagnostic Equipment Nationwide View Details →

Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q

St. Jude Medical, Cardiac Rhythm Management Division

Class I - Dangerous

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

Mar 10, 2022 Implants & Prosthetics Nationwide View Details →

In instances where custom reference ranges were configured on the device post installation, a possibility to inadvertently apply changes to reference range values was found on software versions 2.59.3 and all earlier versions, which can potentially lead to displaying and printing incorrectly-configured reference range values

Jan 20, 2022 Diagnostic Equipment Nationwide View Details →

During the de-installation of an MR system magnet, if all rigging and hardware that attach to the magnet for transportation are not properly installed and secured, the magnet may fall, leading to potential injury.

Mar 4, 2022 Diagnostic Equipment Nationwide View Details →

Artis Q floor, Model Number 10848280

Siemens Medical Solutions USA

Class I - Dangerous

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 the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

Feb 23, 2022 Other Medical Devices Nationwide View Details →

Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q

St. Jude Medical, Cardiac Rhythm Management Division

Class I - Dangerous

Bluetooth malfunction impacting Gallant devices post-implant. The failure causes the device to enter an inductive-only telemetry mode with a loss of Bluetooth communication. The Bluetooth malfunction results in the inability to remotely monitor these devices and resulted in reduced battery longevity.

Mar 10, 2022 Implants & Prosthetics Nationwide View Details →

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 related to the block movements function and manual rotation of the flat detector. Depending on the status of the intervention, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where clinical treatment may be delayed until an additional restart is performed

Feb 25, 2022 Diagnostic Equipment Nationwide View Details →

Artis zee ceiling, Model Number 10094137

Siemens Medical Solutions USA

Class I - Dangerous

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 the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

Feb 23, 2022 Other Medical Devices Nationwide View Details →

Artis Q.zen biplane, Model Number 10848355

Siemens Medical Solutions USA

Class I - Dangerous

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 the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

Feb 23, 2022 Other Medical Devices Nationwide View Details →

Artis Q biplane, Model Number 10848282

Siemens Medical Solutions USA

Class I - Dangerous

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 the message "TUBE HOT, have a break". Several minutes later the system will block X-ray to prevent further damage and display the message "NO XRAY: TUBE TOO HOT".

Feb 23, 2022 Other Medical Devices Nationwide View Details →

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 related to the block movements function and manual rotation of the flat detector. Depending on the status of the intervention, the limited functionality may not be sufficient to continue with treatment as planned. This may result in a situation where clinical treatment may be delayed until an additional restart is performed

Feb 25, 2022 Diagnostic Equipment Nationwide View Details →