Siemens SimView NT and SimView NT with IDI simulation system… — Class II medical device recall Z-0235-2015
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-11-26, distributed nationwide. Siemens became aware of a very rare occurrence where an intended movement of the SimView NT simulation system
| Recall number | Z-0235-2015 |
|---|---|
| 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 | 2014-10-10 |
| Classified | 2014-11-19 |
| Reported by FDA | 2014-11-26 |
| Terminated | 2017-06-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BG, CN, CW, DE, EG, GR, HU, IQ, IT, JO, KR, MY, PL, TH, TR, VN |
| Quantity | 6 |
| Serial numbers | 6001, 6019, 6029, 6032, 6035, 6080 |
| Model numbers | 5496992, 5497016 |
Product
Siemens SimView NT and SimView NT with IDI simulation system components: Product Usage: The intended use of the Radiation Therapy Simulation system is used for simulation of treatment planning prior to the therapeutic treatment of cancer.
Reason for recall
Siemens became aware of a very rare occurrence where an intended movement of the SimView NT simulation system components could not be stopped with usual hand control commands or by use of the collision detection functionality. It is possible that simulation system components could collide with patient and/or system equipment.
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-0235-2015. 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.