AXIOM MULTIX MT — Class II medical device recall Z-2180-2024
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-2180-2024 |
|---|---|
| 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 | 50 units |
| Reason classes | device malfunction |
| Serial numbers | 1003, 1032, 1039, 1060, 1065, 1071, 1076, 1082, 1083, 1085, 1089, 1092, 1104, 1170, 1174, 1181, 1183, 1194, 1304, 1305, 1309, 1310, 1315, 1318, 1323 and 25 more |
Product
AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
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-2180-2024. 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.