Device recall
Z-0674-2024: MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral…
FDA device recall · Class II · Cordis US Corp
Key facts
| Recall number (Z-number) | Z-0674-2024 |
|---|---|
| Recall event | 93617 |
| Product | MYNXGRIP 5F, REF MX5021, Vascular Closure Device (VCD). Used to seal femoral arterial and femoral venous access sites. |
| Product code | MGB |
| Recalling firm | Cordis US Corp |
| Recall class | Class II |
| Status | Open, Classified |
| PMA numbers | P040044 |
| FEI number | 1016427 |
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