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Intuitive recalls da Vinci X and Xi systems over defective capacitors that can cause vision loss or system errors

Intuitive recalled da Vinci X and Xi systems over defective VSC/PSC capacitors that could cause loss of the 3D vision view or system errors. Paired recalls: X (52 systems) and Xi (123 systems). Source: FDA Class 2 device recalls Z-0926-2020 and Z-0925-2020, openFDA enforcement / accessdata.fda.gov.

Occurred 2019-07-26 · Intuitive Surgical · Investigated by FDA

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Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=179352

Common questions

What happened in Intuitive recalls da Vinci X and Xi systems over defective capacitors that can cause vision loss or system errors?
Intuitive recalled da Vinci X and Xi systems over defective VSC/PSC capacitors that could cause loss of the 3D vision view or system errors. Paired recalls: X (52 systems) and Xi (123 systems). Source: FDA Class 2 device recalls Z-0926-2020 and Z-0925-2020, openFDA enforcement / accessdata.fda.gov.
When did this incident occur?
The incident is recorded as occurring on July 26, 2019 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 and Xi systems over defective capacitors that can cause vision loss or system errors?
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 and Xi systems over defective capacitors that can cause vision loss or system errors?
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 and Xi systems over defective capacitors that can cause vision loss or system errors?
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 and Xi systems over defective capacitors that can cause vision loss or system errors.

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Canonical ID a69a4653-6a44-4681-a32d-186c99c69b20