Incident · Recall
Auris Health (J&J) recalls Monarch over a power-cord strain-relief electrical short
Auris Health recalled the Monarch robotic bronchoscopy/urology platform because a power-cord strain-relief defect could cause an electrical short. Paired recalls: endoscopy/bronchoscopy (176 units) and urology (4 units). Source: FDA Class 2 device recalls Z-0051-2025 and Z-0052-2025, accessdata.fda.gov / openFDA enforcement.
Occurred 2024-08-02 · 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 878caa10-e1c0-4bfc-96c7-64798d97a637