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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Siemens Medical Solutions USA, Inc: Radiographic X-Ray Tables Recalled Due to Overheating and Fire Risk

Agency Publication Date: June 25, 2024
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Summary

Siemens Medical Solutions USA, Inc. has recalled approximately 103 units of various Radiographic X-ray Tables, including AXIOM MULTIX, AXIOM Vertix, and MULTIX TOP models, due to a hardware defect. A short circuit in the touch display's power supply unit can cause the component to overheat. This defect poses a fire hazard during medical procedures, potentially endangering both patients and healthcare staff. Consumers should contact the manufacturer immediately to coordinate a resolution.

Risk

A short circuit within the power supply unit of the touch display can lead to excessive heat buildup. This overheating can result in a fire within the medical environment, which could lead to serious injuries or property damage.

What You Should Do

  1. Check the material and serial number on your Siemens radiographic table to see if it is affected by this recall. Affected models include AXIOM MULTIX MT (8395399, 8395415), AXIOM MULTIX MP (8395381, 8395431), AXIOM Vertix MD (MD39543), AXIOM Vertix Solitaire (8627718), MULTIX TOP (475517, 475525), and ZE for Vertix Solitaire (5901900).
  2. Verify your specific serial number against the list of 103 affected units, which include serials such as 1003, 1032, 1039, 1060, 1065, and others listed in the product documentation.
  3. If your device is identified as part of the recall, contact Siemens Medical Solutions USA, Inc. at their Malvern, Pennsylvania headquarters to discuss next steps for service or repair.
  4. Contact your healthcare provider if you have concerns regarding the safety of procedures performed using these specific tables.
  5. For further information or questions regarding this recall, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/repair

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: AXIOM MULTIX MT Radiographic X-ray Table
Model / REF:
8395399
Z-2180-2024
Lot 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
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
Product: AXIOM MULTIX MT Radiographic X-ray Table
Model / REF:
8395415
Z-2181-2024
Lot Numbers:
1010
1011
1015
1105
1117
1124
1126
Product: AXIOM MULTIX MP Radiographic X-ray Table
Model / REF:
8395381
Z-2182-2024
Lot Numbers:
1022
1074
1118
1119
1120
1121
1123
1126
1130
1131
1134
1138
Product: AXIOM MULTIX MP Radiographic X-ray Table
Model / REF:
8395431
Z-2183-2024
Lot Numbers:
1004
1006
1051
1062
1172
1173
1175
1179
1180
1181
1184
1186
1187
1193
1198
1200
1202
1204
1205
1206
Product: AXIOM Vertix MD Radiographic X-ray Table
Model / REF:
MD39543
Z-2184-2024
Lot Numbers:
1040
1020
Product: AXIOM Vertix Solitaire Radiographic X-ray Table
Model / REF:
8627718
Z-2185-2024
Lot Numbers:
1004
1006
1011
1014
Product: MULTIX TOP Radiographic X-ray Table (475517)
Model / REF:
475517
Z-2186-2024
Lot Numbers:
1004
1006
1011
1014
Product: MULTIX TOP Radiographic X-ray Table (475525)
Model / REF:
475525
Z-2187-2024
Lot Numbers:
1523
1585
1897
Product: ZE for Vertix Solitaire Component
Model / REF:
5901900
Z-2188-2024
Lot Numbers:
1239
1241

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94777
Status: Active
Manufacturer: Siemens Medical Solutions USA, Inc
Sold By: Siemens Medical Solutions USA, Inc; authorized medical equipment distributors
Manufactured In: United States
Units Affected: 9 products (50 units; 7 units; 12 units; 20 units; 2 units; 4 units; 3 units; 3 units; 2 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.