Device recall
Z-2329-2016: 6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The…
FDA device recall · Class II · AccessClosure, Inc., A Cardinal Health Company
Key facts
| Recall number (Z-number) | Z-2329-2016 |
|---|---|
| Recall event | 74599 |
| Product | 6F/7F MynxGrip Vascular Closure Device; Product Model MX6721, Product Usage: The 6F/7F MynxGrip Vascular Closure Device is indicated for use to seal femoral arterial and femoral venous access sites while reducing times to hemostasis and ambulation in patients who have undergone diagnostic or… |
| Product code | MGB |
| Recalling firm | AccessClosure, Inc., A Cardinal Health Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 15, 2016 |
| PMA numbers | P040044 |
| FEI number | 3010142363 |
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