Noah Medical
4 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Noah Medical and translate it into plain English — free weekly digest, optional same-day alerts.
- 2025-01-01FDA-DeviceClass IIGalaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedures.
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when the system is not functioning can increase the chance of injury to the tissues of the lung as the scope is withdrawn including the possibility of pneumothorax.
- 2024-12-25FDA-DeviceClass IIGalaxy 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 during procedure, could cause interrupted/aborted procedure, may necessitate manual removal, which could lead to lung injury/pneumothorax.
- 2024-12-18FDA-DeviceClass IIGalaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)
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 with long rigid distal sections may exhibit insertion resistance when bronchoscope bending section significantly articulated.
- 2024-05-08FDA-DeviceClass IIGalaxy 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 patient airways for diagnostic and therapeutic procedures.
Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.
Get notified about new Noah Medical recalls
Free weekly digest. We email when a new federal recall affects Noah Medical or anything else in your household.
Get the Sunday Brief