{"id":"f230d6be-58ed-44c8-8970-5c448de939b8","slug":"fda-recall-davinci5-foot-pedal-2025","filingNumber":"Z-1325-2025","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":"2025-02-26T12:00:00.000Z","decisionDate":"2025-03-12T12:00:00.000Z","status":"recalled","clearanceScope":"Recall of da Vinci 5 console foot pedal over a spring failure that could lead to unintended energy activation; 2025.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - da Vinci 5 foot pedal (2025)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"5c278679-5662-4b93-80f7-2ff4556870d0","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:14.886Z","updatedAt":"2026-06-05T15:35:53.964Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"2e6d8061-3ddd-438e-abcf-a58d0aefbcb9","modelId":"45105ba4-1c1f-4121-9ad4-bb912db1dcfc","regulatoryFilingId":"f230d6be-58ed-44c8-8970-5c448de939b8","createdAt":"2026-06-04T23:17:15.045Z","model":{"slug":"intuitive-da-vinci","modelName":"da Vinci (and Ion)"}}]}