# FDA recall Z-2196-2019

> **Siemens Medical Solutions USA, Inc** · Class II · device recall initiated 2019-07-10.

## Product

Lantis 8.3 Commander, Model # 8148178 - 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 for recall

Potentially affected by the Microsoft Windows Remote Desktop Protocol (RDP) vulnerability

## Distribution

State    WV  NY  PA  FL  OK  FL  NJ  NY  IL  WY  NY  GA  NY  PA  PA  AL  NJ  NY  ***updated 8/14/19***  OH  NC

## Key facts

- **Recall number:** Z-2196-2019
- **Recalling firm:** Siemens Medical Solutions USA, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-10
- **Report date:** 2019-08-14
- **Termination date:** 2020-06-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Malvern, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2196-2019

## Citation

> AI Analytics. FDA recall Z-2196-2019. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2196-2019. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*