Siemens Lantis 6.1 Commander Recalled for Windows RDP Vulnerability
Siemens Medical Solutions is recalling two Lantis 6.1 Commander units due to a Microsoft Windows Remote Desktop Protocol vulnerability.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically corresponds to a moderate severity level. The source text does not report any injuries, illnesses, or deaths, and the hazard is a software vulnerability rather than a direct physical or biological risk.
Plain-English summary
Siemens Medical Solutions USA, Inc. is recalling two units of the Lantis 6.1 Commander, Model # 5493072. The recall is issued because the product is potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability.
The Lantis Treatstation is used by radiation therapists to deliver treatment to patients using the mevatron and available accessories. The system supports functions such as auto sequencing and intensity modulation. The affected units are distributed across multiple states, including West Virginia, New York, Pennsylvania, Florida, Oklahoma, New Jersey, Illinois, Wyoming, Georgia, Alabama, Ohio, and North Carolina.
The source text does not specify the exact remediation steps or consumer actions required beyond the recall notice. The recall number is Z-2195-2019.
The recalled product
- Product
- Lantis 6.1 Commander, Model # 5493072 - 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, set
- Manufacturer
- Siemens Medical Solutions USA, Inc
- Hazard
- Affected units
- 2
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Serial Number 93-1158 93-0803
Distribution
Part of a larger recall action
This product is one of 4 recalled by Siemens Medical Solutions USA, Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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