Elekta, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2917-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

MOSAIQ Oncology Information System

Product Classification:

Class II

Date Initiated: August 3, 2018

Date Posted: August 29, 2018

Recall Number: Z-2917-2018

Event ID: 80764

Reason for Recall:

Order Status Remains Approved When Should Indicate Complete.

Status: Terminated

Product Quantity: 185

Code Information:

Software Build(s) 2.64 SP3 and higher

Distribution Pattern:

AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, WA, WI, WV, and WY Australia, Canada, Ireland, New Zealand, Portugal, Singapore, South Africa, Spain, Sweden, and United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated