{"id":"95018cab-0548-4b32-ab7d-fcca5b56c238","slug":"fda-recall-asensus-senhance-arm-2023","filingNumber":null,"filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"a3a097cb-a5db-4ffd-b421-5eb14335dbcf","filingDate":"2023-09-15T12:00:00.000Z","decisionDate":"2023-10-30T12:00:00.000Z","status":"recalled","clearanceScope":"Class I recall of the Asensus Senhance system after a software malfunction caused an uncontrolled arm movement; 2023.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - Asensus Senhance (2023, Class I)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"e6425590-be49-4ab6-994b-0ff020bae90b","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:17.764Z","updatedAt":"2026-06-05T15:35:52.003Z","applicantCompany":{"id":"a3a097cb-a5db-4ffd-b421-5eb14335dbcf","slug":"asensus-surgical","name":"Asensus Surgical"},"modelLinks":[{"id":"c0acac18-216d-43de-945b-ff67aa560ef5","modelId":"abadf566-b528-4b44-be3e-418ca078e920","regulatoryFilingId":"95018cab-0548-4b32-ab7d-fcca5b56c238","createdAt":"2026-06-04T23:17:17.929Z","model":{"slug":"asensus-senhance","modelName":"Senhance"}}]}