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Mevion Medical Systems, Inc. recalls MEVION S250i
Recalled January 16, 2019 · FDA recall Z-0705-2019 · Mevion Medical Systems
Hazard
Treatment is allowed to continue (via partials) in situations where dDose1 interlock has tripped · FDA Class II
Units
1 unit
Sold at
DC
Description
Treatment is allowed to continue (via partials) in situations where dDose1 interlock has tripped
Product
MEVION S250i
Manufacturer(s)
Mevion Medical Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →