Dynarex CGA870 All Brass Oxygen Regulator, All Brass - 0-25 LPM, Barb & 2-DISS Outlet, UPC recall — FDA Z-1955-2018
The device is equipped with a dial that has an inaccurate flow rate indicator.
Overview of recall records associated with Dynarex Corporation, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The device is equipped with a dial that has an inaccurate flow rate indicator.
This page summarizes recall records in which the official source identifies Dynarex 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.