Elekta, Inc.: Medical Device Recall in 2014 - (Recall #: Z-1869-2014)

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 MOSAIQ is an oncology information system used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be used where ever radiotherapy and/or chemotherapy are prescribed.

Product Classification:

Class II

Date Initiated: May 29, 2014

Date Posted: July 2, 2014

Recall Number: Z-1869-2014

Event ID: 68386

Reason for Recall:

MOSAIQ does not re-calculate the agent volume when the user changes the ordering dose (to other than what was calculated) prior to saving the order.

Status: Terminated

Product Quantity: 101

Code Information:

Released builds 2.50.04D5 and higher

Distribution Pattern:

Worldwide Distribution - USA (nationwide) including Puerto Rico and the states of AL, AK, AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, IA, KY, LA, ME, MD, MA, MI, MO, MT, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TX, VT, VA and WA,. and the countries of Australia, Canada, New Zealand and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated