Dynarex Oxygen Regulator Recalled for Inaccurate Flow Rate Indicator
Dynarex Corporation is recalling 15 CGA870 oxygen regulators because the dial has an inaccurate flow rate indicator. The devices were distributed in Massachusetts and New Jersey.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard is an inaccurate flow rate indicator, which is a functional defect but does not involve a high-risk pathogen, structural failure, or reported injuries, fitting the Moderate category for minor labeling or functional errors.
Plain-English summary
Dynarex Corporation is recalling 15 units of the CGA870 All Brass Oxygen Regulator (Model Number 5227, UPC: 616784522715). The recall is due to a defect where the device is equipped with a dial that has an inaccurate flow rate indicator.
The affected devices were distributed in the United States to the states of Massachusetts and New Jersey. The specific lot number for the recalled units is 37979.
Consumers who have this product should stop using it and contact Dynarex Corporation for further instructions.
The recalled product
- 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 ga
- Manufacturer
- Dynarex Corporation
- Hazard
- Affected units
- 15
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot number: 37979
Distribution
Related recalls
Same manufacturer · Dynarex Corporation
See all →- ModerateDynarex Recalls Specimen Containers Due to Incorrect Sterile Labeling
FDA (Devices) · 2016-07-06
- ModerateDynarex CPR Shield Recalled for Incorrect Orientation Labeling
FDA (Devices) · 2014-08-06
Other medical device recalls
- HighIMRIS ORT200 Operating Room Table Recalled for Mechanical Failure Risk
FDA (Devices) · 2026-09-02
- HighIMRIS ORT300 Operating Room Table Recalled for Mechanical Failure Risk
FDA (Devices) · 2026-09-02
- HighMedline Recalls 71 Convenience Kits Due to Contaminated Component
FDA (Devices) · 2026-09-02
- HighMedline Recalls 419 Surgical Kits Due to Contaminated Component
FDA (Devices) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02