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Noah Medical

Products: endoluminal-robot. Risk band: High RobotRisk index 45.0/100 (severity- and time-weighted incidents) · ranked 3 of 25 among Medical robotics companies with incidents (173 tracked).

Analyst brief

Noah Medical shows three FDA Class II recalls of the same Galaxy System platform, spanning March 2024 through September 2025, all severity 3 and all recall-type entries. The repetition of recalls against the same device family (Galaxy System, including a controller-specific recall) indicates a recurring rather than isolated issue with that product line. Noah Medical's index of 45.0 ranks 3 of 25 companies in Medical robotics with incident history. The record is entirely regulator-driven (FDA recall classifications), with a consistent severity level and no escalation to injury or fatality entries, and the pattern points to a persistent single-product quality issue rather than a broad safety event.

Risk index

45.0/100RobotRisk index

22.1/100Median index across the 25 Medical robotics companies with incident history (173 tracked, 148 with none)

3 of 25Rank in Medical robotics (of 25 with incident history)

HighRisk band

Incident timeline

Comparisons over time

Per-type breakdown

Incident type	Unique incidents	Share
recall	3	100%

Unique incident list

3 unique incidents on file for this company.

Sev	Date	Type	Location	Incident	Source
S3	12 Sep 2025	recall	—	FDA Class II recall: Brand Name: Galaxy System · Brand Name: Galaxy System	openFDA enforcement
S3	28 Oct 2024	recall	—	FDA Class II recall: Galaxy System (GAL-001). · Galaxy System (GAL-001).	openFDA enforcement
S3	09 Mar 2024	recall	—	FDA Class II recall: Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) · Galaxy System REF GAL-001 (specifically GAL-019, Wired Contr	openFDA enforcement