MEVION S250i — Class II medical device recall Z-2406-2020
Terminated recall by Mevion Medical Systems, Inc., reported 2020-07-01, distributed in DC, FL, MO, NJ, OH, OK. Couch Correction moves sent after using a 3D CT scan are partially lost if the previous correction sent or rec
| Recall number | Z-2406-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mevion Medical Systems, Inc., Littleton, MA, United States |
| Recall initiated | 2020-05-15 |
| Classified | 2020-06-22 |
| Reported by FDA | 2020-07-01 |
| Terminated | 2020-12-11 |
| Distributed | DC, FL, MO, NJ, OH, OK |
| Countries outside the US | NL |
| Quantity | 8 units |
| UPC / GTIN / UDI-DI | 00864366000100, 00864366000124 |
Product
MEVION S250i, MEVION S250; Proton Radiation Treatment System
Reason for recall
Couch Correction moves sent after using a 3D CT scan are partially lost if the previous correction sent or recorded had some of the Couch Correction checkboxes turned off
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-2406-2020. 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.