{"url_path":"/fda/device/recalls/Z-2318-2026","section_key":"summary","section_title":"DEVICE Recall: GE Medical Systems, LLC — Allia Moveo angiographic X-ray system","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-04-20","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2318-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"GE Medical Systems, LLC"},"word_count":102,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2318-2026\n\n**Recalling firm:** GE Medical Systems, LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-04-20\n**Report date:** 2026-06-17\n\n## Product\nAllia Moveo angiographic X-ray system\n\n## Reason\nGE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.\n\n## Affected lots\nUDI-DI: 00198953052488; Serial Numbers: C4-25-001, C4-25-002, C4-26-001, C4-26-002, C4-26-004, C4-26-005\n\n## Distribution\nWorldwide - US Nationwide distribution."}