Device recall
Z-1585-2025: Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter…
FDA device recall · Class I · Conavi Medical Inc.
Key facts
| Recall number (Z-number) | Z-1585-2025 |
|---|---|
| Recall event | 96444 |
| Product | Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product Description: Common Name: Diagnostic intravascular catheter Description: The Novasight Hybrid catheter is a 3Fr single use, sterile device, which will be able to perform transluminal… |
| Product code | OBJ |
| Recalling firm | Conavi Medical Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K172258 |
| FEI number | 3012198618 |
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