{"url_path":"/fda/device/recalls/Z-2406-2026","section_key":"summary","section_title":"DEVICE Recall: Elekta, Inc. — MOSAIQ Oncology Information System","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-21","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2406-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Elekta, Inc."},"word_count":110,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2406-2026\n\n**Recalling firm:** Elekta, Inc.\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-21\n**Report date:** 2026-06-17\n\n## Product\nMOSAIQ Oncology Information System\n\n## Reason\nSoftware may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.\n\n## Affected lots\nSoftware Version: MOSAIQ 3.2/UDI: 07340201500071\n\n## Distribution\nWorldwide - 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, \tHong Kong, India, Israel, Italy, Japan, Lithuania, Malta, Mexico, Netherlands, Pakistan, \tPanama, Poland, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom."}