AXIOM Vertix Solitaire — Class II medical device recall Z-2185-2024
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2024-07-03, distributed nationwide. Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
| Recall number | Z-2185-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2024-05-31 |
| Classified | 2024-06-25 |
| Reported by FDA | 2024-07-03 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| Reason classes | device malfunction |
| 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 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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2185-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.