Mevatron M2/Primus Mid-Energy PRIMUS HI — Class II medical device recall Z-1489-2017
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2017-03-29, distributed nationwide. Software update
| Recall number | Z-1489-2017 |
|---|---|
| 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 | 2017-02-14 |
| Classified | 2017-03-20 |
| Reported by FDA | 2017-03-29 |
| Terminated | 2017-12-18 |
| Distributed | Nationwide (US) |
| Quantity | 80 systems |
| Reason classes | software |
| Model numbers | 1940035, 4504200 |
Product
Mevatron M2/Primus Mid-Energy PRIMUS HI
Reason for recall
Software update
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-1489-2017. 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.