Elekta, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0731-2017)

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:

MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.

Product Classification:

Class II

Date Initiated: December 2, 2016

Date Posted: December 21, 2016

Recall Number: Z-0731-2017

Event ID: 75853

Reason for Recall:

Edits to Particle field definition parameters may not be saved when the field definition window is saved.

Status: Terminated

Product Quantity: 47

Code Information:

Versions 2.60 an higher

Distribution Pattern:

Worldwide Distribution-US (nationwide) to states of: FL, IL, MO, NJ, OH, OK, TN, TX, VA, and countries of: Italy, Japan, South Korea, Sweden and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated