Elekta, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0221-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

MOSAIQ Product Usage: MOSAIQ is an oncology information system used to manage workflows for treatment planing and delivery. It supports information flow among healthcare facility personnel and can be used wherever radiotherapy and/or chemotherapy are prescribed.

Product Classification:

Class II

Date Initiated: November 3, 2014

Date Posted: November 26, 2014

Recall Number: Z-0221-2015

Event ID: 69656

Reason for Recall:

A problem can exist in MOSAIQ resulting in the display of incorrect numeric data due to a dose rounding error on printed reports.

Status: Terminated

Product Quantity: 15

Code Information:

MOSAIQ Release 2.60.257

Distribution Pattern:

US Nationwide Distribution in the states of AZ. CO, IL, MD, MO, NY, OK, OR, PA, RI, TX, VA

Voluntary or Mandated:

Voluntary: Firm initiated