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Incident · Recall

Intuitive recalls da Vinci EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals

Placing excessive tissue in the jaws of the EndoWrist Vessel Sealer Extend before sealing and transection could result in an insufficient seal, a bleeding and hemostasis risk during surgery. Source: FDA Class 2 device recall Z-1209-2022 (approx. 140,519 boxes / 843,113 units), accessdata.fda.gov.

Occurred 2022-03-03 · Intuitive Surgical · Investigated by FDA

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Track Intuitive recalls da Vinci EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals

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Sources (1)

  1. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=192095

Common questions

What happened in Intuitive recalls da Vinci EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals?
Placing excessive tissue in the jaws of the EndoWrist Vessel Sealer Extend before sealing and transection could result in an insufficient seal, a bleeding and hemostasis risk during surgery. Source: FDA Class 2 device recall Z-1209-2022 (approx. 140,519 boxes / 843,113 units), accessdata.fda.gov.
When did this incident occur?
The incident is recorded as occurring on March 3, 2022 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 EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals?
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 EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals?
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 EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals?
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 EndoWrist Vessel Sealer Extend instruments over risk of insufficient vessel seals.

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Canonical ID 7b04937b-617b-4efc-9f73-315b5f93af62