Device recall
Z-1955-2018: Dynarex CGA870 All Brass Oxygen Regulator, All Brass - 0-25 LPM, Barb & 2-DISS…
FDA device recall · Class II · Dynarex Corporation
Key facts
| Recall number (Z-number) | Z-1955-2018 |
|---|---|
| Recall event | 80058 |
| 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… |
| Product code | CAN |
| Recalling firm | Dynarex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2018 |
| FEI number | 2431014 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database