Incident · Recall
Intuitive Surgical recalls 144 da Vinci 5 systems over surgeon console motor connector failure
FDA Class 2 recall Z-0964-2026 (firm-initiated Aug 21 2024; posted Dec 19 2025): Error 23062 due to partially damaged or failed surgeon console column motor connector. Causes ergonomics to lock — viewer, headrest, armrest, and pedal tray position cannot be adjusted until da Vinci is restarted.
May lead to delay, aborted, or alternate procedure. FDA-determined cause: Device Design. 144 units in commerce across 30+ US states. Remedy: motor module sub-assembly replacement.
Occurred 2024-08-21 · da Vinci (and Ion) at Hong Kong, China · Intuitive Surgical · Hong Kong, China · Surgical robots · Investigated by FDA
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Sources (1)
- FDA (Class 2 Recall Z-0964-2026) · https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=217489
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Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
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Last reviewed 2026-08-09
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Canonical ID 624582b8-cfa2-46dd-8c01-01b623905a93