Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2184-2024 — 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

U.S. FDA — Device Enforcement · United States · 2024-05-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2184-2024
Date of alert
2024-05-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Siemens Medical Solutions USA, Inc
Product category
device
Product type
Devices
Reported risk: Short circuit in the power supply unit (PSU) of the Touch Display may lead to overheating and fire
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.