Device recall
Z-1403-2018: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644…
FDA device recall · Class II · Teleflex Medical Europe Ltd
Key facts
| Recall number (Z-number) | Z-1403-2018 |
|---|---|
| Recall event | 79670 |
| Product | Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in respiratory and anesthesia circuits to connect two or more components of a breathing system. |
| Product code | BZA |
| Recalling firm | Teleflex Medical Europe Ltd |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 4, 2021 |
| FEI number | 3007134520 |
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