_Incident · Recall_

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

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

- **Occurred:** 2018-03-07
- **Kind:** `recall`
- **Status (derived):** active
- **Company:** [Intuitive Surgical](/companies/intuitive-surgical.md) (id: `e5127536-0ff2-4f0e-8488-64994cb2ffc7`)

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.

## Sources (0)

_No sources on file._

## 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.


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