ClearanceBrief
Recall Z-2184-2024 ยท IZZ Table, Radiographic, Non-Tilting, Powered

Siemens Medical Solutions USA, Inc

AXIOM Vertix MD - The Vertix MD Trauma has been specially designed for examining emergency and accident patients as well as for use in outpatient departments. Material Number: MD39543

DateJun 25, 2024 (initiated May 31, 2024)
StatusOpen, Classified
ReasonShort circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Root causeUnder Investigation by firm
ActionSiemens 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 per
Quantity2 units
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.