Z-2185-2024 Class II Ongoing
FDA device recall Z-2185-2024 was initiated by Siemens Medical Solutions USA, Inc on May 31, 2024 and is designated Class II. Reason for recall: Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire The recall status is ongoing. Affected quantity: 4 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 3, 2024
- Initiation Date
- May 31, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4 units
Product Description
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
Reason for Recall
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Distribution Pattern
US Nationwide distribution.
Code Information
UDI-DI: N/A Serial Numbers: 1004 1006 1011 1014
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2185-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026