{"url_path":"/fda/device/recalls/Z-2477-2026","section_key":"summary","section_title":"DEVICE Recall: GE Medical Systems, LLC — Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-05-01","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2477-2026%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":137,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-2477-2026\n\n**Recalling firm:** GE Medical Systems, LLC\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-05-01\n**Report date:** 2026-06-24\n\n## Product\nGiraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500\n\n## Reason\nGE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury.\n\n## Affected lots\nSerial Numbers: 5452896 801057486 800977619 801093759 5584569 5587625 5367527 5603110 5371240 5497382\n\n## Distribution\nWorldwide - US Nationwide distribution."}