{"id":"efb0eaec-fac6-4027-a139-a367b6b76591","slug":"fda-recall-davinci-sureform-gray-reload-2026","filingNumber":"Z-1855-2026","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":"2026-03-11T12:00:00.000Z","decisionDate":"2026-05-01T12:00:00.000Z","status":"recalled","clearanceScope":"Recall of the da Vinci 8mm SureForm 30 Gray stapler reload after incomplete staple formation associated with a patient death; 2026.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - da Vinci SureForm Gray reload (2026)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"e5e34795-0e48-49e1-8427-019ec1b1a86b","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:16.372Z","updatedAt":"2026-06-05T15:35:53.650Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"f50e22c0-882d-4153-a411-28c9182a4814","modelId":"45105ba4-1c1f-4121-9ad4-bb912db1dcfc","regulatoryFilingId":"efb0eaec-fac6-4027-a139-a367b6b76591","createdAt":"2026-06-04T23:17:16.524Z","model":{"slug":"intuitive-da-vinci","modelName":"da Vinci (and Ion)"}}]}