Noah Medical recalls
Noah Medical appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2025-12-03.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 5 |
|---|---|
| Published | 2024-05-08 to 2025-12-03 |
| By agency | FDA Device (5) |
| By classification | Class II (5) |
| By status | ongoing (5) |
| Distribution named in notices | CA, CO, CT, ID, IL, IN, MA, MD, MN, MO, NC, NJ, NY, OH, PA, SC, TN, US, VA, WI, WV, WY |
Recalls
- Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its access…
FDA Device · Class II · 2025-12-03 · Noah Medical
Reason: Due to Users not having access to the Instructions for Use/User Manual due to it being password protected. - Galaxy System (GAL-001)
FDA Device · Class II · 2025-01-01 · Noah Medical
Reason: 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 t… - Galaxy System (GAL-001)
FDA Device · Class II · 2024-12-25 · Noah Medical
Reason: 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… - Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)
FDA Device · Class II · 2024-12-18 · Noah Medical
Reason: 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 forc… - Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its accessories are intended to provide bronchosco…
FDA Device · Class II · 2024-05-08 · Noah Medical
Reason: Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.