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Noah Medical

Robot types: Endoluminal. Risk band: Elevated RobotRisk index 44.7/100 (severity- and time-weighted incidents) · ranked 3 of 25 among Medical robotics companies with incidents (274 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. 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

44.7/100RobotRisk index

21.8/100Median index across the 25 Medical robotics companies with incident history (274 tracked, 249 with none)

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

ElevatedRisk band

Products and robot types

Industries: Medical robotics · Sectors: Hospitals and Health Care

Risk is scored per product and robot type: each incident is attributed to the product it names, or to the company's matching robot type.

Robot type	Share of company risk	Rank within type
Endoluminal	100%	2 of 2

Product	Robot type	Status	Incidents	Index
Galaxy	Endoluminal	shipping	3	44.7

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