Elekta, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2052-2016)

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

Product Classification:

Class II

Date Initiated: June 17, 2016

Date Posted: July 6, 2016

Recall Number: Z-2052-2016

Event ID: 74378

Reason for Recall:

It is possible that that the selected Plan-of-the Day could be accidently changed by scrolling the mouse wheel up and down and inadvertently selecting another plan.

Status: Terminated

Product Quantity: 69

Code Information:

Versions 2.62 and higher

Distribution Pattern:

US Distribution including Puerto Rico and to the states of : AK, AZ, CA, FL, GA, IL, IN, LA, MD, MI, MO, NJ, NY, OH, OR, PA, TN, TX, UT, VA, WA, and to the countries of : Canada, Denmark, Finland, Germany, Israel, Japan, Netherlands, Norway, Sweden, United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated