{"id":"7ee2d461-04d6-4f6b-9a30-e770ffb5ff1d","slug":"fda-recall-davinci-instrument-carriage-2023","filingNumber":"Z-1262-2023","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":null,"decisionDate":"2023-03-16T12:00:00.000Z","status":"recalled","clearanceScope":"Recall of da Vinci X/Xi over a loose instrument carriage caused by an out-of-spec component; 2023.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - da Vinci X/Xi instrument carriage (2023)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"4ed8c518-03f3-47dc-8ae4-fcdce4462922","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:14.432Z","updatedAt":"2026-06-05T15:35:53.025Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"ea7ee16b-342a-46e6-ad22-6583b0fce3af","modelId":"45105ba4-1c1f-4121-9ad4-bb912db1dcfc","regulatoryFilingId":"7ee2d461-04d6-4f6b-9a30-e770ffb5ff1d","createdAt":"2026-06-04T23:17:14.583Z","model":{"slug":"intuitive-da-vinci","modelName":"da Vinci (and Ion)"}}]}