FDAOctober 25, 2024device

Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy System (GAL-001)

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

The hazard

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

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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