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

Recall Z-2186-2024 — MULTIX TOP - Intended Use: The Multix TOP I PRO Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number:475517

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-2186-2024
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

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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.