Z-0409-2017 Class II Terminated

Recalled by Mevion Medical Systems, Inc. — Littleton, MA

FDA device recall Z-0409-2017 was initiated by Mevion Medical Systems, Inc. on October 31, 2016 and is designated Class II. Reason for recall: Completing Setup Without Program Move Complete Can Cause An Isocenter Error The recall status is terminated (terminated June 29, 2017). Affected quantity: 6 units.

Recall Details

Product Type
Devices
Report Date
November 23, 2016
Initiation Date
October 31, 2016
Termination Date
June 29, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6 units

Product Description

MEVION S250 Product Usage: Proton Radiation Therapy

Reason for Recall

Completing Setup Without Program Move Complete Can Cause An Isocenter Error

Distribution Pattern

US Nationwide in the states of FL, MO, NJ and OK

Code Information

Serial NUmbers: S250-0001 through S250-0006