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

Recall Z-2197-2019 — Lantis Commander, Model # 4503178 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the patient using the mevatron and all available accessories. This entails selecting a patient, selecting today s treatment for that patient, setting up and delivering

U.S. FDA — Device Enforcement · United States · 2019-07-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2197-2019
Date of alert: 2019-07-10
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: Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability

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.

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.

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