FDA recall Z-2921-2020

Siemens Medical Solutions USA, Inc · Class II · device

Product

Siemens Sensis Vibe Hemo system in combination with the MicroPodTM EtCO2 module-diagnostic and administrative tool supporting hemodynamic catheterization and/or electrophysiology studies, for cardiac as well as interventional Radiology.

Reason for recall

The connector linking the EtCO2 module to the HemoBox may break and become damaged, if the connector is re-attached to the HemoBox in this damaged state, under certain incorrect pin alignment conditions, the HemoBox may stop functioning and all vital signs are lost

Distribution

US Nationwide distribution.

Key facts

Status
Terminated
Initiation date
2020-07-24
Report date
2020-09-09
Termination date
2021-11-02
Voluntary/Mandated
Voluntary: Firm initiated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2921-2020