FDA Device recall Z-2195-2019
Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the…
- FDA Device
- Class II
- terminated
- Published 2019-08-14
On 2019-08-14 the FDA classified a Class II recall of Lantis 6.1 Commander, Model # 5493072 - Product Usage: Lantis Treatstation is to allow the radiation therapist to deliver treatment to the… by Siemens Medical Solutions Usa, citing potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2195-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-07-10 |
| Published | 2019-08-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | AL, FL, GA, IL, NC, NJ, NY, OH, OK, PA, WV, WY |
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, setting up and delivering the treatment fields and recording the delivered treatment. Treatstation supports auto sequencing, a process of automatically downloading a group of fields or segments from the verification and record system to the control of the linear accelerator sequentially, without user intervention. In addition, Lantis Treatstation supports intensity modulation, a process of shaping, modifying and moving the beam around a target to maximize the dose at the target and minimize the dose to normal structures.
Reason
Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability
Identifiers
| code_info | Serial Number 93-1158 93-0803 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2195-2019%22
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