Class II

Medical Device Recall: MOSAIQ Oncology Information System

Elekta, Inc. · May 21, 2026

Reason for Recall

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

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, Switzerland, Taiwan, Thailand, Turkey, United Kingdom.

States Affected

NATIONWIDE

Quantity Affected

12 programs

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2406-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Elekta, Inc. Medical Device Recall: MOSAIQ Oncology Information System | SafeCheck