FDA Device recall Z-2181-2024
AXIOM MULTIX MT - 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 MT - 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-2181-2024 |
| 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 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: 8395415
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: 1010 1011 1015 1105 1117 1124 1126 |
|---|
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-2181-2024%22
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