{"url_path":"/fda/device/recalls/Z-2643-2026","section_key":"summary","section_title":"DEVICE Recall: Siemens Medical Solutions USA, Inc — ARTIS icono floor. Model Number: 11327700.","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-2643-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"Siemens Medical Solutions USA, Inc"},"word_count":99,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2643-2026\n\n**Recalling firm:** Siemens Medical Solutions USA, Inc\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\nARTIS icono floor. Model Number: 11327700.\n\n## Reason\nPotential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.\n\n## Affected lots\nModel Number: 11327700. UDI-DI: 4056869149325. Serial Numbers: 174132, 174128, 174085, 174152, 174056, 174055, 174083, 174121, 174122, 174087, 174044, 174061, 174099, 174058, 174063, 174150, 174126, 174125, 174096, 174145, 174101, 174065, 174076, 174078, 174091, 174149, 174059, 174073, 174081, 174067.\n\n## Distribution\nUS Nationwide distribution."}