FDA Medical Device · Z-2406-2026

MOSAIQ Oncology Information System

Class II · Ongoing

Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.

Affected lots / codes — check yours against thisSoftware Version: MOSAIQ 3.2/UDI: 07340201500071

Recalling firm: Elekta, Inc., Atlanta, GA
Classification: Class II (temporary or reversible harm possible)
Status: Ongoing
Quantity: 12 programs
Distribution: Worldwide - US Nationwide distribution in the states of WI, FL, LA, NY, NY, NJ, KS, FL, IA, NM, TX and the countries of Bahrain, Belgium, Canada, China, Denmark, France, Germany, Hong Kong, India, Israel, Italy, Japan, Lithuania, Malta, Mexico, Netherlands, Pakistan, Panama, Poland, Spain, Sweden…
Recall initiated: May 21, 2026
Classified: June 11, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2406-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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