FDA recall Z-2186-2024

Siemens Medical Solutions USA, Inc · Class II · device

Product

MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517

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-2186-2024