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Recall Observatory FDA recall evidence

Device 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

Z-1426-2022

June 15, 2022

Class II

Product summary

Firm
Siemens Medical Solutions USA, Inc
Event
Event 90504
Status
Ongoing
Classification
Class II
Quantity
13 units
Official record key
device-enforcement:Z-1426-2022

Official wording

Reason: 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.

Code information: UDI-DI: 04056869010205 Serial Numbers: 123021, 123055, 123056, 123058, 122042, 123004, 122006, 122026, 122029, 123047, 123053, 122011, 121014.

Distribution pattern: US Nationwide Distribution AZ FL KY MI OH PR TX

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.