Recall Z-2188-2024— Siemens Medical Solutions USA, Inc
Class II · Ongoing
Class II FDA medical device recall by Siemens Medical Solutions USA, Inc, initiated 2024-05-31. FDA's recall record names no specific 510(k) clearance for this event. Product: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900. Reason: Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire.
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-05-31
- Firm location
- Malvern, PA, United States
Product description
ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
Reason for recall
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Data sourced from openFDA. This site is unofficial and independent of the FDA.