X-ray Table Touch Display Power Supply Fire Hazard
Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II medical device with a potential fire hazard from a power supply short circuit. No injuries or deaths have been reported, making this a risk-of-harm product where injury has not yet been reported, qualifying for a High severity score per the rubric.
Plain-English summary
Siemens Medical Solutions USA, Inc. is recalling the AXIOM MULTIX MT Radiographic X-ray Patient Table due to a potential fire hazard. The Touch Display power supply unit contains a component that may experience a short circuit, which could lead to overheating and fire.
The AXIOM MULTIX MT is a patient table used with Siemens Multix PRO and TOP Systems radiographic devices. This recall affects 50 units distributed nationwide. The affected serial numbers are: 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, 1325, 1331, 1348, 1359, 1382, 1395, 1398, 1423, 1443, 1444, 1447, 1449, 1452, 1453, 1468, 1498, 1500, 1508, 1509, 1512, 1513, 1515, 1516, 1525, 1531.
Healthcare facilities and operators with affected serial numbers should immediately stop using the equipment and contact Siemens Medical Solutions USA, Inc. for further instructions or replacement.
The recalled product
- 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
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Affected units
- 50
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 9 recalled by Siemens Medical Solutions USA, Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 9 products in this recall →Related recalls
Same manufacturer · Siemens Medical Solutions USA, Inc
See all →- HighARTIS icono floor Medical Imaging System Detector Movement Loss Recall
FDA (Devices) · 2026-07-08
- HighARTIS Icono Ceiling Model 11328100 Loss of Movement Capability Recall
FDA (Devices) · 2026-07-08
- ModerateARTIS icono biplane medical imaging system detector lift malfunction
FDA (Devices) · 2026-07-08
- ModerateARTIS icono ceiling medical imaging monitor suspension system
FDA (Devices) · 2026-07-08
- HighARTIS pheno systems may display zero dose while dose is applied
FDA (Devices) · 2026-06-10
Same hazard · short circuit
See all →- Severe
- SevereNissan Recalls 2026 Leaf Vehicles Due to High Voltage Battery Fire Risk
NHTSA · 2026-03-25
- SevereVolvo EX30 high voltage battery may short circuit and overheat
NHTSA · 2026-02-20
- SevereFord Escape and Lincoln Corsair plug-in hybrid battery cells may short
NHTSA · 2026-02-17
- HighWestern Star battery to starter stud may short circuit
NHTSA · 2026-02-11