Natus Manufacturing Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product recall — FDA Z-1143-2021
The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.
Overview of recall records associated with Natus Manufacturing Limited, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.
This page summarizes recall records in which the official source identifies Natus Manufacturing Limited 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.