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FDAFDA · Food and drugs·Recall number Z-2185-2024

AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: 8627718

Published July 3, 2024 · Recall initiated: May 31, 2024

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Recall details

Manufacturer
Siemens Medical Solutions USA, Inc
Distributor
US Nationwide distribution.
Lot
UDI-DI: N/A Serial Numbers: 1004 1006 1011 1014
Risk classification
Class II
Area (FDA)
device
Country
United States

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