{"id":"7d3b9829-3b9a-48a6-b027-f9f944c39631","slug":"fda-recall-davinci-sureform-fragment-2022","filingNumber":"Z-0340-2023","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":null,"decisionDate":"2022-11-30T12:00:00.000Z","status":"recalled","clearanceScope":"Recall of da Vinci Xi 8mm SureForm 30 stapler over staple-deployment failure / fragment risk; 2022.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - da Vinci SureForm 30 stapler (2022)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"912e22fb-a60f-4f18-8f06-0e8304054fcd","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:13.968Z","updatedAt":"2026-06-05T15:35:53.332Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"a245ef52-526f-4c34-859b-c074d24cceb2","modelId":"45105ba4-1c1f-4121-9ad4-bb912db1dcfc","regulatoryFilingId":"7d3b9829-3b9a-48a6-b027-f9f944c39631","createdAt":"2026-06-04T23:17:14.120Z","model":{"slug":"intuitive-da-vinci","modelName":"da Vinci (and Ion)"}}]}