Elekta, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0169-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR) used for oncology workflow management. It lets users supply electronic patient charts and assemble care plans, order diagnostic tests, and prescribe medications. It also lets users import, view, annotate, manipulate, enhance, manage, and archive images.

Product Classification:

Class II

Date Initiated: September 18, 2012

Date Posted: November 7, 2012

Recall Number: Z-0169-2013

Event ID: 63335

Reason for Recall:

A patient was seriously mistreated after a user made and saved an inadvertent change to the definition of a treatment filed in MOSAIQ.

Status: Terminated

Product Quantity: 300

Code Information:

Version 2.00 to 2.41

Distribution Pattern:

Worldwide distribution: USA (nationwide) and country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated