Siemens LANTIS Oncology Information System Servers — Class II medical device recall Z-1282-2015
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2015-03-25, distributed nationwide. There is a potential safety risk when using LANTIS server software with operating systems with which it has no
| Recall number | Z-1282-2015 |
|---|---|
| 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 | 2015-01-21 |
| Classified | 2015-03-16 |
| Reported by FDA | 2015-03-25 |
| Terminated | 2015-07-30 |
| Distributed | Nationwide (US) |
| Quantity | 87 |
| Reason classes | software |
| Serial numbers | 93-0037, 93-0063, 93-0096, 93-0102, 93-0141, 93-0159, 93-0222, 93-0261, 93-0272, 93-0278, 93-0370, 93-0385, 93-0393, 93-0398, 93-0416, 93-0452, 93-0454, 93-0456, 93-0475, 93-0483, 93-0487, 93-0490, 93-0501, 93-0533, 93-0564 and 62 more |
| Model numbers | 04503178, 05493072, 08148178 |
Product
Siemens LANTIS Oncology Information System Servers; allows the radiation therapist to deliver treatment to patient using the MEVATRON and all available accessories
Reason for recall
There is a potential safety risk when using LANTIS server software with operating systems with which it has not been validated or released which can lead to an incorrect treatment to the patient.
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-1282-2015. 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.