Ziehm Imaging Recalls
14 recalls on record · January 1, 2014 to May 24, 2017 · Medical Devices
Recalls by year
14
16
17
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 24, 2017Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
Hazard: During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision2, Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Solo, Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision RFD, Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision RFD Mot, Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
August 31, 2016Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
Hazard: Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision R C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vision C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.
January 1, 2014Medical DevicesFDA
Ziehm Imaging Inc recalls Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Hazard: Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.