FDAMarch 9, 2024device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to a misaligned calibration of the wired controller that may result in unintended motion of the scope.

What to do

FDA enforcement status: Ongoing

Brands named

noah medicalnoah

UPCs

00850048825048

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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