# FDA recall Z-1955-2018

> **Dynarex Corporation** · Class II · device recall initiated 2018-05-08.

## Product

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.

## Reason for recall

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

## Distribution

US Distribution to the states of : MA and NJ

## Key facts

- **Recall number:** Z-1955-2018
- **Recalling firm:** Dynarex Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-08
- **Report date:** 2018-06-06
- **Termination date:** 2018-09-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Orangeburg, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1955-2018

## Citation

> AI Analytics. FDA recall Z-1955-2018. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1955-2018. Source: US FDA. Licensed CC0.

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