{"url_path":"/fda/device/recalls/Z-2641-2026","section_key":"summary","section_title":"DEVICE Recall: Siemens Medical Solutions USA, Inc — ARTIS icono biplane. Model Number: 11327600.","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-2641-2026%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":154,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2641-2026\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 biplane. Model Number: 11327600.\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: 11327600. UDI-DI: 4056869063317. Serial Numbers: 184246, 184241, 184086, 184178, 184108, 184099, 184070, 184127, 184095, 184167, 184184, 184205, 184199, 184221, 184126, 184047, 184093, 184044, 184096, 184214, 184100, 184119, 184073, 184188, 184134, 184150, 184081, 184153, 184085, 184243, 184117, 184045, 184159, 184151, 184177, 184079, 184087, 184169, 184116, 184157, 184163, 184123, 184090, 184118, 184140, 184230, 184224, 184195, 184248, 184225, 184190, 184106, 184046, 184078, 184200, 184142, 184138, 184166, 184152, 184113, 184186, 184196, 184105, 184102, 184147, 184120, 184121, 184124, 184211, 184233, 184216, 184050, 184067, 184112, 184122, 184220, 184089, 184097, 184234, 184103, 184098, 184084, 184183, 184179, 184109\n\n## Distribution\nUS Nationwide distribution."}