AXIOM Vertix Solitaire - The Vertix MD Trauma has been recall
AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in…
Why was AXIOM Vertix Solitaire - The Vertix MD Trauma has been recalled?
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: N/A Serial Numbers: 1004 1006 1011 1014
- Product
- AXIOM Vertix Solitaire - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 4 units
- Distribution
- US Nationwide distribution.
- Recall date
- July 3, 2024
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)