Home / Recalls / Medical Devices
Siemens Medical Solutions USA, Inc recalls Sensis Vibe Combo with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizat
Recalled July 27, 2022 · FDA recall Z-1426-2022 · Siemens Medical Solutions USA
Hazard
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting in no vital signs being available. · FDA Class II
Units
13 units
Sold at
US Nationwide Distribution AZ FL KY MI OH PR TX
Description
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting in no vital signs being available.
Product
Sensis Vibe Combo with software version VD12A. A diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology Model: 11007642
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →