Device recall
Z-1384-2021: Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30 mm Vascular…
FDA device recall · Class II · Covidien, LP
Key facts
| Recall number (Z-number) | Z-1384-2021 |
|---|---|
| Recall event | 87475 |
| Product | Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30 mm Vascular 8 mm - Short Item Code: SIGSDS30CTV |
| Product code | CDW |
| Recalling firm | Covidien, LP |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 12, 2024 |
| 510(k) numbers | K191070 |
| FEI number | 1219930 |
At a glance
- 1–9 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