Class II — Dynarex Corporation
| Recalling firm | DYNAREX CORP. |
|---|---|
| Registered facility | DYNAREX CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The device is equipped with a dial that has an inaccurate flow rate indicator. |
| 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. |
| Quantity | 15 devices |
| Distribution | US Distribution to the states of : MA and NJ |
| Initiated | 2018-05-08 |
| Classified | 2018-05-29 |
| Terminated | 2018-09-18 |
| Recall number | Z-1955-2018 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Dynarex Corporation (Z-1955-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80058/
Alerts for DYNAREX CORP.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.