Mevion Medical Systems, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0767-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

MEVION S250 Radiation therapy system

Product Classification:

Class II

Date Initiated: November 18, 2015

Date Posted: February 17, 2016

Recall Number: Z-0767-2016

Event ID: 72210

Reason for Recall:

The treatment table positioning belt can slip gear positions, resulting in deviation of patient setup and treatment positions from the time of slippage until the discovery of slippage and the halting of treatment.

Status: Terminated

Product Quantity: 4

Code Information:

Manufacturing Lot or Serial Number: S250-0004

Distribution Pattern:

US nationwide distribution including FL, NJ, OK, and MO.

Voluntary or Mandated:

Voluntary: Firm initiated