Device recall
Z-2657-2026: 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI…
FDA device recall · Class II · Bard Access Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2657-2026 |
|---|---|
| Recall event | 99096 |
| Product | 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119 The intended use of the Short-Term Dialysis Catheter is attaining temporary/short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, or apheresis therapy via the jugular… |
| Product code | PXI |
| Recalling firm | Bard Access Systems, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K030268 |
| FEI number | 3006260740 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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