Device recall
Z-0950-2022: Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous…
FDA device recall · Class II · Resource Optimization & Innovation LLC
Key facts
| Recall number (Z-number) | Z-0950-2022 |
|---|---|
| Recall event | 89793 |
| Product | Regard IV Start Kit for preparing and/or dressing a peripheral vein intravenous access site |
| Product code | LRS |
| Recalling firm | Resource Optimization & Innovation LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2022 |
| FEI number | 3004513970 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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