Device recall
Z-2239-2023: Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava…
FDA device recall · Class II · Argon Medical Devices, Inc
Key facts
| Recall number (Z-number) | Z-2239-2023 |
|---|---|
| Recall event | 92585 |
| Product | Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO, RxOnly, CE 2797 |
| Product code | DTK |
| Recalling firm | Argon Medical Devices, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K133243 |
| FEI number | 1625425 |
At a glance
- 1–9 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