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Incident · Recall

Intuitive recalls da Vinci X systems over a high rate of ACJ board failure

Intuitive recalled da Vinci X systems because a defective component caused a high rate of Arm Control Joint (ACJ) board failure. 108 ACJ boards across 35 systems. Source: FDA Class 2 device recall Z-2341-2018, openFDA enforcement / accessdata.fda.gov.

Occurred 2018-03-07 · Intuitive Surgical · Investigated by FDA

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Track Intuitive recalls da Vinci X systems over a high rate of ACJ board failure

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Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=180599

Common questions

What happened in Intuitive recalls da Vinci X systems over a high rate of ACJ board failure?
Intuitive recalled da Vinci X systems because a defective component caused a high rate of Arm Control Joint (ACJ) board failure. 108 ACJ boards across 35 systems. Source: FDA Class 2 device recall Z-2341-2018, openFDA enforcement / accessdata.fda.gov.
When did this incident occur?
The incident is recorded as occurring on March 7, 2018 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
Who was involved in Intuitive recalls da Vinci X systems over a high rate of ACJ board failure?
The incident is recorded as involving Intuitive Surgical on the DEPLOY registry. No specific robot model is linked to this incident in the registry.
Has anyone responded to Intuitive recalls da Vinci X systems over a high rate of ACJ board failure?
No responses to this incident are recorded on the DEPLOY registry. Operators, manufacturers, or affected parties can submit responses to the editorial team; absence is not a guarantee no response was issued.
What is the current status of Intuitive recalls da Vinci X systems over a high rate of ACJ board failure?
This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.
Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09

Verification posture

Verified

High confidence

Review state

Stable

Last reviewed 2026-08-09

Sources by quality tier

1
primary-fda-database
FDA database

The framework is documented at /methodology. Corrections at /corrections. Reviewer: DEPLOY editorial team.

Methodology surface for Intuitive recalls da Vinci X systems over a high rate of ACJ board failure.

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Canonical ID 460ae57b-3870-40a3-8fbf-a2802da11068