Siemens X-ray Table Recalled for Fire Hazard in Power Supply
Siemens recalls AXIOM MULTIX MT radiographic X-ray tables due to a short circuit in the power supply unit that may cause overheating and fire. 7 units are affected nationwide.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
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: FDA Class II recall with potential fire hazard from electrical short circuit in medical device. No injuries or hospitalizations have been reported, making this a risk-of-harm product where injury has not yet occurred, meeting the High severity criterion.
Plain-English summary
Siemens Medical Solutions USA, Inc. is recalling the AXIOM MULTIX MT radiographic X-ray table (Material Number: 8395415), a patient table designed for use with Siemens Multix PRO and TOP Systems radiographic devices. Seven units with serial numbers 1010, 1011, 1015, 1105, 1117, 1124, and 1126 are included in this recall.
The recall is prompted by a short circuit in the power supply unit (PSU) of the Touch Display, which may lead to overheating and fire. This creates a potential safety hazard to patients, medical personnel, and the facility.
The affected units have been distributed nationwide throughout the United States. Healthcare facilities currently using any of the affected serial numbers should immediately cease use of the equipment.
Facilities should contact Siemens Medical Solutions USA, Inc. for repair, replacement, or return instructions for the affected devices. This recall has been assigned number Z-2181-2024 by the FDA.
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: 8395415
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Category
- Medical Device — X-ray Table
- Affected units
- 7
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- UDI-DI: N/A Serial Numbers: 1010 1011 1015 1105 1117 1124 1126
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.
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