Device recall
Z-2369-2020: Regard SRHS Central Line Kit, Sterile, 20/case - Product Usage: The Saline Flush…
FDA device recall · Class II · Resource Optimization & Innovation LLC
Key facts
| Recall number (Z-number) | Z-2369-2020 |
|---|---|
| Recall event | 85632 |
| Product | Regard SRHS Central Line Kit, Sterile, 20/case - Product Usage: The Saline Flush Syringes are intended to be used only for the flushing of indwelling of vascular access devices. |
| Product code | PEZ |
| Recalling firm | Resource Optimization & Innovation LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 23, 2022 |
| FEI number | 3004513970 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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