Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Galaxy System REF GAL-001 (specifically GAL-019 Recalled by Noah Medical Due to Due to a misaligned calibration of the wired...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Noah Medical directly.
Affected Products
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 patient airways for diagnostic and therapeutic procedures.
Quantity: 17 wired controllers
Why Was This Recalled?
Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Noah Medical
Noah Medical has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report