Siemens LANTIS System — Class II medical device recall Z-1840-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-07-02, distributed nationwide. There is a potential risk when using LANTIS OIS System client software with operating systems for which it has
| Recall number | Z-1840-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2014-05-06 |
| Classified | 2014-06-20 |
| Reported by FDA | 2014-07-02 |
| Terminated | 2014-12-15 |
| Distributed | Nationwide (US) |
| Quantity | 108 |
| Reason classes | software |
| Serial numbers | 93-0037, 93-0063, 93-0096, 93-0102, 93-0141, 93-0159, 93-0222, 93-0231, 93-0261, 93-0262, 93-0272, 93-0278, 93-0314, 93-0326, 93-0370, 93-0385, 93-0393, 93-0398, 93-0416, 93-0452, 93-0454, 93-0456, 93-0475, 93-0483, 93-0487 and 83 more |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1840-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.