# FDA recall Z-0693-2025

> **Noah Medical** · Class II · device recall initiated 2024-10-25.

## Product

Galaxy System (GAL-001)

## Reason for recall

Bronchoscopic system uninterruptable power may have defective component, may cause power supply short circuit/trip protective circuit breakers causing sudden, unrecoverable power loss, which could occur while system is on mains or internal battery power; if during procedure, could cause interrupted/aborted procedure, may necessitate manual removal, which could lead to lung injury/pneumothorax.

## Distribution

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

## Key facts

- **Recall number:** Z-0693-2025
- **Recalling firm:** Noah Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-10-25
- **Report date:** 2024-12-25

- **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-0693-2025

## Citation

> AI Analytics. FDA recall Z-0693-2025. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-0693-2025. Source: US FDA. Licensed CC0.

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