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Incident · Recall

Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)

FDA Class II recall Z-2720-2024 (posted 2024-09-04): instrument-cart-arm screw issue in the Intuitive Ion Endoluminal System associated with potential uncontrolled instrument-arm motion.

Occurred 2024-09-04 · da Vinci (and Ion) · Intuitive Surgical · Surgical robots · Investigated by FDA

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Incident records on DEPLOY are compiled from public sources (regulatory filings, news reports, and operator disclosures) and reflect what has been reported and tracked to date. They are not legal findings, determinations of fault, or safety ratings, and may be updated as new information is verified. See the sources below for the underlying references.

Machine-readable surfaces

Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?start_search=1&recallnumber=Z-2720-2024

Common questions

What happened in Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)?
FDA Class II recall Z-2720-2024 (posted 2024-09-04): instrument-cart-arm screw issue in the Intuitive Ion Endoluminal System associated with potential uncontrolled instrument-arm motion.
When did this incident occur?
The incident is recorded as occurring on September 4, 2024 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.
What robot was involved in Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)?
da Vinci (and Ion) by Intuitive Surgical is the recorded robot involved in this incident.
Has anyone responded to Intuitive Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)?
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 Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024)?
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 2026-07-21

Verification posture

Verified

High confidence

Review state

Stable

Last reviewed 2026-07-21

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 Ion Endoluminal System recall: instrument-cart-arm screw issue (Z-2720-2024).

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Canonical ID 85536738-fc38-4f48-9af6-d5e236f7a108