FDA Device recall Z-1840-2014

Siemens LANTIS System

• FDA Device
• Class II
• terminated
• Published 2014-07-02

On 2014-07-02 the FDA classified a Class II recall of Siemens LANTIS System by Siemens Medical Solutions Usa, citing there is a potential risk when using LANTIS OIS System client software with operating systems for which it has not been validated and released, resulting in incorrectly stored dat….

Read the official FDA Device notice

Product

Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander The intended use of the linear accelerator is to deliver x-ray radiation for therapeutic treatment of cancer.

Reason

There is a potential risk when using LANTIS OIS System client software with operating systems for which it has not been validated and released, resulting in incorrectly stored data, such as treatment records, and LANTIS database corruption.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1840-2014%22

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