_Incident · Injury_

# Auris Monarch: patient developed pneumothorax post-procedure requiring chest-tube placement (FDA MAUDE)

Canonical ID: `e9497f9d-30c5-4dd4-bdfb-e1f11ae1e102`

- **Occurred:** 2026-04-30
- **Kind:** `injury`
- **Status (derived):** active
- **Company:** [Auris Health](/companies/auris-health.md) (id: `df69ac5c-53c1-4fa6-94d2-8f377e9bf87c`)

An FDA MAUDE injury report describes an Auris Monarch endoscopy platform case in which the patient developed a pneumothorax after the procedure, requiring chest-tube placement. Source: FDA MAUDE MDR key 25166932, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

## Sources (0)

_No sources on file._

## Common questions

### What happened in Auris Monarch: patient developed pneumothorax post-procedure requiring chest-tube placement (FDA MAUDE)?

An FDA MAUDE injury report describes an Auris Monarch endoscopy platform case in which the patient developed a pneumothorax after the procedure, requiring chest-tube placement. Source: FDA MAUDE MDR key 25166932, openFDA device event / accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE.

### When did this incident occur?

The incident is recorded as occurring on April 30, 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: patient developed pneumothorax post-procedure requiring chest-tube placement (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: patient developed pneumothorax post-procedure requiring chest-tube placement (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: patient developed pneumothorax post-procedure requiring chest-tube placement (FDA MAUDE)?

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


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