Dynarex Corporation: Medical Device Recall in 2018 - (Recall #: Z-1955-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Dynarex CGA870 All Brass Oxygen Regulator, All Brass - 0-25 LPM, Barb & 2-DISS Outlet, UPC: 616784522715, Model Number 5227 A pressure regulator is a device, often called a pressure-reducing valve, that is intended for medical purposes and that is used to convert a medical gas pressure from a high variable pressure to a lower, more constant working pressure. This device includes mechanical oxygen regulators.

Product Classification:

Class II

Date Initiated: May 8, 2018

Date Posted: June 6, 2018

Recall Number: Z-1955-2018

Event ID: 80058

Reason for Recall:

The device is equipped with a dial that has an inaccurate flow rate indicator.

Status: Terminated

Product Quantity: 15 devices

Code Information:

Lot number: 37979

Distribution Pattern:

US Distribution to the states of : MA and NJ

Voluntary or Mandated:

Voluntary: Firm initiated