---
title: "Noah Medical Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search Noah Medical recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/noah-medical/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# Noah Medical recall records

**4** reported ongoing

4 records in this archive. Latest source date Oct 28, 2024.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## Records and reported status

Oct 28, 2024 FDA device enforcement

### [Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedures.](https://isitonrecall.com/recall/fda-device-z-0742-2025-galaxy-system-gal-001-intended-to-provide-bronchoscopic-visualization-of-and-access-to-patient-airwa/)

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...

Class II Reported ongoing

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

[Official source for Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0742-2025%22)

Oct 25, 2024 FDA device enforcement

### [Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)](https://isitonrecall.com/recall/fda-device-z-0679-2025-galaxy-bronchoscope-product-galb-001-used-with-instructions-for-use-part-10000752-part-of-the-noah-m/)

Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner diameter/length greater or equal to 1100mm) will pass through if scope channel positioned in sharp bend (approx. greater than 100-deg.), excessive force may result in tissue injury/pneumoth...

Class II Reported ongoing

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

[Official source for Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of th...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0679-2025%22)

Oct 25, 2024 FDA device enforcement

### [Galaxy System (GAL-001)](https://isitonrecall.com/recall/fda-device-z-0693-2025-galaxy-system-gal-001/)

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...

Class II Reported ongoing

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

[Official source for Galaxy System (GAL-001)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0693-2025%22)

Mar 9, 2024 FDA device enforcement

### [Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its accessories are intended to provide bronchoscopic visualization of and access to pat...](https://isitonrecall.com/recall/fda-device-z-1734-2024-galaxy-system-ref-gal-001-specifically-gal-019-wired-controller-the-galaxy-system-and-its-accessorie/)

Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.

Class II Reported ongoing

Distribution: U.S. Nationwide distribution in the states of CA, IN, MD, MO, OH, and PA.

[Official source for Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its acce...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1734-2024%22)

## Reasons in these listed records

- 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 inc...
- Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner diameter/length greater or equal to 1100mm) will pass through if scope channel positioned in sharp bend (approx. greater than 100-deg.), excessive force may result in tissue injury/pneumothorax; instruments wi...
- 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, c...
- Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.

These examples come from this result page and are not a ranking of every recall reason.

## Checking Noah Medical

### Is there a recall on noah medical right now?

This archive contains 4 records, including 4 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search Noah Medical](https://isitonrecall.com/check/?q=Noah%20Medical) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
