_Incident · Malfunction_

# Auris Monarch bronchoscope: Navigation EM error at the docking station, scope removed (FDA MAUDE)

Canonical ID: `5ee1871a-3b83-4056-a9d3-7048c272c175`

- **Occurred:** 2026-05-08
- **Kind:** `malfunction`
- **Status (derived):** active
- **Company:** [Auris Health](/companies/auris-health.md) (id: `df69ac5c-53c1-4fa6-94d2-8f377e9bf87c`)

An FDA MAUDE malfunction report describes an Auris Monarch bronchoscope displaying a Navigation EM error when connected to the docking station, leading to the scope being removed. Source: FDA MAUDE MDR key 25229150, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

## Sources (0)

_No sources on file._

## Common questions

### What happened in Auris Monarch bronchoscope: Navigation EM error at the docking station, scope removed (FDA MAUDE)?

An FDA MAUDE malfunction report describes an Auris Monarch bronchoscope displaying a Navigation EM error when connected to the docking station, leading to the scope being removed. Source: FDA MAUDE MDR key 25229150, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

### When did this incident occur?

The incident is recorded as occurring on May 8, 2026 on the DEPLOY registry. The date reflects the underlying real-world event, not the registry record's creation date.

### Who was involved in Auris Monarch bronchoscope: Navigation EM error at the docking station, scope removed (FDA MAUDE)?

The incident is recorded as involving Auris Health on the DEPLOY registry. No specific robot model is linked to this incident in the registry.

### Has anyone responded to Auris Monarch bronchoscope: Navigation EM error at the docking station, scope removed (FDA MAUDE)?

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 Auris Monarch bronchoscope: Navigation EM error at the docking station, scope removed (FDA MAUDE)?

This incident is an active record on the DEPLOY registry; no retraction or correction has been issued.


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