Z-0409-2017 Class II Terminated
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