Device recall
Z-1330-2025: Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F…
FDA device recall · Class II · Cordis US Corp
Key facts
| Recall number (Z-number) | Z-1330-2025 |
|---|---|
| Recall event | 96272 |
| Product | Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems. |
| Product code | DQY |
| Recalling firm | Cordis US Corp |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K021593 |
| FEI number | 1016427 |
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