FDAJuly 12, 2024device

Ion Endoluminal System, REF: 380748-65

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential that the robotic system's instrument cart arm may contain screws that may potentially fail which could result in uncontrolled motion of a catheter inside a patient's airways.

What to do

FDA enforcement status: Ongoing

Brands named

intuitive surgicalintuitive

UPCs

00886874116234

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Ion Endoluminal System, REF: 380748-65 — Recall Details · AllClear