Z-2180-2024 Class II Ongoing
FDA device recall Z-2180-2024 was initiated by Siemens Medical Solutions USA, Inc on May 31, 2024 and is designated Class II. Reason for recall: Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire The recall status is ongoing. Affected quantity: 50 units.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 3, 2024
- Initiation Date
- May 31, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 50 units
Product Description
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
Reason for Recall
Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Distribution Pattern
US Nationwide distribution.
Code Information
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
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2180-2024
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026