Siemens recalls Lantis 6.1 Commander model 5493072 due to potential Microsoft Windows RDP vulnerability. Affected units may be at risk of security breaches. Contact for remedy details.
Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
Siemens is recalling its Lantis 6.1 Commander medical imaging device because it could be vulnerable to a security flaw in the Windows Remote Desktop Protocol. This could allow unauthorized access to patient data if the device is connected to a network.
The device uses a Windows Remote Desktop Protocol (RDP) that could be exploited by hackers to gain unauthorized access to patient data. This vulnerability is a security risk if the device is connected to a network.
Radiation therapists using the Lantis 6.1 Commander model 5493072 for patient treatment are most at risk. The recall affects specific units with serial numbers starting with 93-1158 or 93-0803.
Check for the model number 5493072 on the device. Serial numbers starting with 93-1158 or 93-0803 indicate affected units. The device is used by radiation therapists for delivering patient treatments.
Identify the model number on the device, which should be 5493072 for affected units.
Check the serial number, which starts with 93-1158 or 93-0803 for affected units.
The Lantis 6.1 Commander model 5493072 may be vulnerable to a security flaw in the Windows Remote Desktop Protocol (RDP) that could allow unauthorized access to patient data.
Check the model number and serial number to see if your device is affected. Contact Siemens for further instructions.
The recall record does not specify a remedy or fix for the vulnerability.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2195-2019 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2195-2019 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.
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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.
