{"url_path":"/fda/device/recalls/Z-2647-2026","section_key":"summary","section_title":"DEVICE Recall: RAYSEARCH LABORATORIES AB — RayCare 2024A SP4. Oncology Information Systems.","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-20","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2647-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"RAYSEARCH LABORATORIES AB"},"word_count":91,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2647-2026\n\n**Recalling firm:** RAYSEARCH LABORATORIES AB\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-20\n**Report date:** 2026-07-08\n\n## Product\nRayCare 2024A SP4. Oncology Information Systems.\n\n## Reason\nBeam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.\n\n## Affected lots\nSoftware Version 8.0.4.60077, UDI 0735000201089120241218, Expiration Date: 2030-01-24.\n\n## Distribution\nWorldwide - US Nationwide distribution."}