{"id":"ab00f3fe-4c62-4081-9195-ecae2d2f502d","slug":"fda-recall-stryker-mako-software-2024","filingNumber":"Z-1910-2024","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","filingDate":"2024-05-28T12:00:00.000Z","decisionDate":"2024-05-28T12:00:00.000Z","status":"recalled","clearanceScope":"Software correction for Stryker Mako Total Knee over 'error #3' codes during registration; 2024.","sources":[{"url":"https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm","title":"FDA Medical Device Recall - Stryker Mako Total Knee software (2024)","sourceName":"FDA Recall Database (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":"481430cf-9415-451a-b2b0-00f582214f99","reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-04T23:17:16.835Z","updatedAt":"2026-06-05T15:35:55.303Z","applicantCompany":{"id":"661fbd42-9fcb-4d47-8a74-7a23d161d57b","slug":"stryker","name":"Stryker"},"modelLinks":[{"id":"153ad0c0-b69e-4f7f-a582-630ae6a2dec7","modelId":"b3a006a0-d844-4fb4-b4d9-dd6f148c0958","regulatoryFilingId":"ab00f3fe-4c62-4081-9195-ecae2d2f502d","createdAt":"2026-06-04T23:17:16.986Z","model":{"slug":"stryker-mako","modelName":"Mako"}}]}