FDA recall Z-2188-2024

Siemens Medical Solutions USA, Inc · Class II · device

Product

ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900

Reason for recall

Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire

Distribution

US Nationwide distribution.

Key facts

Status
Ongoing
Initiation date
2024-05-31
Report date
2024-07-03
Voluntary/Mandated
Voluntary: Firm initiated
Location
Malvern, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2188-2024