{"id":"7d253b17-cc5d-4ea8-ae61-874365e0fef2","slug":"fda-recall-davinci-instrument-arm-diagnostic-2026","filingNumber":"Z-1232-2026","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":null,"decisionDate":"2026-02-02T12:00:00.000Z","status":"recalled","clearanceScope":"Recall of da Vinci X/Xi/5 over a software error that let instrument arms continue after failing a boot-up diagnostic; 2025.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - da Vinci instrument-arm diagnostic (2025)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":"Slug corrected 2025 -> 2026: FDA recall Z-1232-2026 posted 2026-02-02 (primary-source-anchored). Old path 301-redirected by Rover.","relatedIncidentId":"7d97d0f6-5ac1-4b4b-9727-27ed83b907a2","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:15.371Z","updatedAt":"2026-06-05T16:55:30.678Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"3ad1d497-669e-44ec-a2c8-940365c13870","modelId":"45105ba4-1c1f-4121-9ad4-bb912db1dcfc","regulatoryFilingId":"7d253b17-cc5d-4ea8-ae61-874365e0fef2","createdAt":"2026-06-04T23:17:15.524Z","model":{"slug":"intuitive-da-vinci","modelName":"da Vinci (and Ion)"}}]}