PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: July 3, 2024 Initiated: May 31, 2024 #Z-2184-2024

Product Description

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

Details

Units Affected
2 units
Distribution
US Nationwide distribution.
Location
Malvern, PA

Frequently Asked Questions

What product was recalled?
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. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 2 units.
Why was this product recalled?
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Which agency issued this recall?
This recall was issued by the FDA Devices on July 3, 2024. Severity: Moderate. Recall number: Z-2184-2024.