Z-2180-2024Class II

AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens...

Name: Z-2180-2024 AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens...
Creator: Siemens Medical Solutions USA, Inc
Published: 2024-05-31
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2024-05-31 / Open, Classified

FDA source

Siemens Medical Solutions USA, Inc began a 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 radiographic devices... on 2024-05-31. FDA classified it as Class II and gives the reason as "Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-2180-2024
Classification: Class II
Status: Open, Classified
Initiated: 2024-05-31
Posted: 2024-06-25
Recalling firm: Siemens Medical Solutions USA, Inc.
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
Product code: IZZ Table, Radiographic, Non-Tilting, Powered
Reason for recall: Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
FDA root cause: Under Investigation by firm
Action: Siemens issued Urgent Medical Device Correction Letter (XP008/24/S) to the Attention: Director of Diagnostic Imaging and/ or Radiology Laboratory on 5/31/24. Letter states reason for recall, health risk, and action to take: What steps can the user take to avoid the possible risks associated with this issue? It is recommended to switch off the system / Touch Display when it is not in use and is unattended. How will the issue be resolved? To ensure continued safe operation of your system and to provide safeguards for the life of the system, the Siemens Healthineers Service Organization will perform the replacement of the PSU of the Touch Display via UI XP006/24/S beginning in the second quarter (June) of 2024. This replacement will be provided to you free of charge. Based on our investigation you can continue to use your system following the recommendation to switch off the system / Touch Display when it is not in use and is unattended. Our service organization will contact you to arrange a date to perform this corrective action once it is available. Please feel free to contact our Customer Care Center at 1-800-888-7436 for an earlier appointment beginning in June 2024. Please review, understand, and confirm acknowledgement of the information and instructions outlined in this Customer Safety Advisory Notice. Please respond within 14 days of receiving this notification.
Quantity in commerce: 50 units
Distribution: US Nationwide distribution.
Product codes and lots: UDI-DI: N/A Serial 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

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2180-2024
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2180-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2181-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2182-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2183-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2184-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2185-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2186-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2187-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25
Z-2188-2024	Class II	Ongoing	Voluntary: Firm initiated	2024-07-03	2024-06-25

Product code IZZ

K971452Class IIMultix Top/pro Radiographic X-Ray TableSiemens Medical Solutions USA, Inc. / cleared 1997-05-14

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)