Siemens recalls Lantis Commander model 4503178 due to potential Microsoft Windows Remote Desktop Protocol vulnerability. Affected units may be at risk of security issues.
Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
Siemens is recalling its Lantis Commander model 4503178 because it could be vulnerable to a Microsoft Windows Remote Desktop Protocol (RDP) security flaw. This risk could allow unauthorized access to the device, though the specific impact isn't detailed in the recall.
The device could be vulnerable to a security flaw in the Microsoft Windows Remote Desktop Protocol (RDP). This might allow unauthorized remote access to the system, potentially compromising patient data or device functionality.
Radiation therapists using the Lantis Commander model 4503178 for patient treatment may be affected. Patients and staff at facilities using this specific model are at risk if the vulnerability is exploited.
Check for the model number 4503178 on the device. Affected units have serial numbers starting with 93- (e.g., 93-0759, 93-0648).
Verify the model number on your Lantis Commander device to confirm it is 4503178.
Reach out to Siemens Medical Solutions USA, Inc for further guidance on security risks.
The recall addresses a potential security vulnerability, not a direct impact on patient treatment. Siemens has not specified how this affects clinical use.
Check for the model number 4503178 and serial numbers starting with 93- on your device.
Siemens recommends contacting them directly for security guidance, as no specific remedy is stated in the recall.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2197-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2197-2019 from Siemens. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
