{"id":"2b756794-b623-4cc7-a5d9-2ad15aff4fec","slug":"fda-recall-intuitive-ion-2024","filingNumber":"Z-2720-2024","filingType":"fda_recall","jurisdiction":"us_fda","applicantCompanyId":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","filingDate":"2024-07-12T12:00:00.000Z","decisionDate":"2024-09-04T12:00:00.000Z","status":"recalled","clearanceScope":"Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue associated with potential uncontrolled instrument-arm motion.","sources":[{"url":"https://api.fda.gov/device/recall.json?search=product_res_number:Z-2720-2024","title":"FDA recall Z-2720-2024","sourceName":"openFDA (primary)"}],"verificationPosture":"verified","capFlagNotes":null,"relatedIncidentId":null,"reviewStatus":"reviewed","deprecatedAt":null,"deprecationReason":null,"createdAt":"2026-06-05T16:55:33.248Z","updatedAt":"2026-06-05T18:22:52.647Z","applicantCompany":{"id":"e5127536-0ff2-4f0e-8488-64994cb2ffc7","slug":"intuitive-surgical","name":"Intuitive Surgical"},"modelLinks":[{"id":"814d1cac-c0c6-4bb4-ad00-937084c7ca12","modelId":"0e2f5d6f-8ce6-4726-9301-d438ecf732bc","regulatoryFilingId":"2b756794-b623-4cc7-a5d9-2ad15aff4fec","createdAt":"2026-06-05T17:43:05.979Z","model":{"slug":"intuitive-ion","modelName":"Ion Endoluminal System"}}]}