{"id":"63a35db7-3ab5-44ac-9f48-2d681ca736ff","slug":"recall-2026-02-18-intuitive-surgical","kind":"recall","headline":"FDA Class 2 recall: da Vinci 5 viewer display firmware issue causing loss of 3D surgical field","summary":"FDA classified Class 2 recall for da Vinci 5 (IS5000). Viewer Display manufactured with outdated firmware may result in loss of one display and loss of 3D surgical field depth perception. 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Viewer Display manufactured with outdated firmware may result in loss of one display and loss of 3D surgical field depth perception. Recall Z-1428-2026.","identifier":"63a35db7-3ab5-44ac-9f48-2d681ca736ff","datePublished":"2026-02-18T12:00:00.000Z","articleSection":"recall","publisher":{"@id":"https://deploy.report/#organization"},"author":{"@id":"https://deploy.report/#organization"}},"framework_metadata":{"framework_schema_version":"0.1.0","verification_status":"unreviewed","maturity_stage":null,"lifecycle_state":null,"architectural_position":{"cohort":null,"sub_cohorts":[]},"within_cohort_verified_vs_claimed_pair":null,"cap_flags":[],"verification_depth":{"sources_count":1,"primary_source_types":["primary-fda-database"]}}}