Incident · Recall
Auris Health (J&J) recalls Monarch over unanticipated robotic arm positioning toward patient-left
Auris Health recalled the Monarch bronchoscopy platform because a software issue could cause unanticipated robotic-arm positioning toward patient-left, risking contact with the patient or endotracheal tube. 173 units. Source: FDA Class 2 device recall Z-1383-2026, openFDA enforcement / accessdata.fda.gov.
Occurred 2026-01-21 · Auris Health · Investigated by FDA
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Methodology: Verified · 1 source (1 primary) · last reviewed 2026-08-09
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Last reviewed 2026-08-09
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Canonical ID 7c94b4de-e7b2-4c72-b105-abe5d51feb74