Official recall record
Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-10-25
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00850048825048
- Brand on record
- Noah Medical
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 3 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2025-09-12 · US FDA — Medical Devices
Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy S - 2024-03-09 · US FDA — Medical Devices
Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) The Galaxy System and its accessories are intended - 2024-10-28 · US FDA — Medical Devices
Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for diagnosti
Other recalls from this brand
- 2024-10-28 · US FDA — Medical Devices
Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for