Orangeburg, NY, United States
Dynarex Corporation recalls
1 recall recorded since 2018, most recently on 8 May 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 8 May 2018
- Terminated
- 18 September 2018
- Reason
- The device is equipped with a dial that has an inaccurate flow rate indicator.
- Distribution
- US Distribution to the states of : MA and NJ
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1955-2018
- 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 f
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.