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Bronchoscope

Noah Medical Corporation · Model 10000769 · UDI-DI 00850048825000

EOQ Prescription
10
510(k) clearances
32,212
Adverse events (207 deaths)
160
Recalls
192
Facilities

Description

The Galaxy System and bronchoscopic is intended to provide visualization of patient airways for diagnostic procedures.

Recalls

DateFirmReason
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-29Olympus Corporation of the AmericasPotential for rubber fragment detachment during use.
2026-01-21Auris Health, IncDevice for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading, application w
2025-12-04Intuitive Surgical, Inc.Due to probe bags that may have a compromised or incomplete sterile pouch seal.
2025-09-12Noah Medical CorporationDue to Users not having access to the Instructions for Use/User Manual due to it being password protected.
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency
2025-09-11Olympus Corporation of the AmericasAdditional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.