Device recall
Z-1902-2025: Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic…
FDA device recall · Class I · Cook Incorporated
Key facts
| Recall number (Z-number) | Z-1902-2025 |
|---|---|
| Recall event | 96848 |
| Product | Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coating. Refer to the… |
| Product code | DQO |
| Recalling firm | Cook Incorporated |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K173289 |
| FEI number | 1820334 |
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