FDA recall Z-2184-2024

Siemens Medical Solutions USA, Inc · Class II · device

Product

AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: MD39543

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-2184-2024