# FDA recall Z-0742-2025

> **Noah Medical** · Class II · device recall initiated 2024-10-28.

## Product

Galaxy System (GAL-001).  Intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedures.

## Reason for recall

Bronchoscopic visualization system power supplies have defective semiconductor components that may fail unexpectedly, which could result in an aborted procedure since it is a non recoverable failure. Manual removal of the bronchoscope when the system is not functioning can increase the chance of injury to the tissues of the lung as the scope is withdrawn including the possibility of pneumothorax.

## Distribution

US: SC, OH, PA, TN, MO, IN, CA, WV, NY, MD, MA, NJ, ID, CT, NC

## Key facts

- **Recall number:** Z-0742-2025
- **Recalling firm:** Noah Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-28
- **Report date:** 2025-01-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** San Carlos, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0742-2025

## Citation

> AI Analytics. FDA recall Z-0742-2025. Retrieved 2026-08-22 from https://api.ai-analytics.org/recall/Z-0742-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*