Mevion Medical Systems, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0705-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

MEVION S250i

Product Classification:

Class II

Date Initiated: October 1, 2018

Date Posted: January 16, 2019

Recall Number: Z-0705-2019

Event ID: 81751

Reason for Recall:

Treatment is allowed to continue (via partials) in situations where dDose1 interlock has tripped

Status: Terminated

Product Quantity: 1 unit

Code Information:

DI: (01)00864366000124 Serial Number: S250i-0007

Distribution Pattern:

Voluntary or Mandated:

Voluntary: Firm initiated