Galaxy System recall — FDA Z-0598-2026
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
Overview of recall records associated with Noah Medical Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
This page summarizes recall records in which the official source identifies Noah Medical Corporation as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.