AXIOM Luminos Agile — Class II medical device recall Z-1001-2023
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2023-01-25. There is potential for the footrest to detach from the patient table during use.
| Recall number | Z-1001-2023 |
|---|---|
| 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 | 2022-12-09 |
| Classified | 2023-01-19 |
| Reported by FDA | 2023-01-25 |
| Quantity | 271 units |
| Reason classes | device malfunction |
Product
AXIOM Luminos Agile
Reason for recall
There is potential for the footrest to detach from the patient table during use.
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-1001-2023. 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.