FDA Enforcement Class II Ongoing

Sensis Vibe systems with software version VD15B in combination with AXIOM Sensis Post Processing Workstation-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as well as surgical studies. Equipped by modules, enabling various configurations. Model: 6648161

Recall: Z-2440-2024 · Reported July 31, 2024

Enforcement

Recall Number
Z-2440-2024
Event ID
94956
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Siemens Medical Solutions USA, Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 31, 2024
Initiation Date
July 3, 2024
Classification Date
July 25, 2024
Address
40 Liberty Blvd, Malvern, PA, 19355-1418, United States

Description

Sensis Vibe systems with software version VD15B in combination with AXIOM Sensis Post Processing Workstation-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as well as surgical studies. Equipped by modules, enabling various configurations. Model: 6648161

Reason

If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.

Code Info

UDI-DI: N/A Serial Numbers: 18904 18906

Distribution

US Nationwide distribution in the states of CA, CT, FL, IA, KS, MA, MI, NJ, TX, VA.

Quantity

2 systems