Device recall
Z-2985-2026: DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide…
FDA device recall · Class I · Bard Access Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2985-2026 |
|---|---|
| Recall event | 99534 |
| Product | DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625200; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625240; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625300; DuoGlide Short-Term Curved Extension Dialysis… |
| Product code | MPB |
| Recalling firm | Bard Access Systems, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K030268, K090102 |
| FEI number | 3006260740 |
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