FDA Device recall Z-2182-2024
AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radi…
- FDA Device
- Class II
- ongoing
- Published 2024-07-03
On 2024-07-03 the FDA classified a Class II recall of AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radi… by Siemens Medical Solutions Usa, citing short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2182-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-31 |
| Published | 2024-07-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395381
Reason
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Identifiers
| code_info | UDI-DI: N/A Serial Numbers: 1022 1074 1118 1119 1120 1121 1123 1126 1130 1131 1134 1138 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2182-2024%22
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