Device recall
Z-0132-2023: Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone…
FDA device recall · Class II · Angiodynamics, Inc.
Key facts
| Recall number (Z-number) | Z-0132-2023 |
|---|---|
| Recall event | 90924 |
| Product | Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling UPN… |
| Product code | LJT |
| Recalling firm | Angiodynamics, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K033473 |
| FEI number | 1319211 |
At a glance
- 1–9 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