Device recall
Z-2663-2026: CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150…
FDA device recall · Class II · Bard Access Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2663-2026 |
|---|---|
| Recall event | 99096 |
| Product | CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 P4254108D PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129353 The PowerMidline" Catheter is intended for short term peripheral access… |
| Product code | PND |
| Recalling firm | Bard Access Systems, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K162900 |
| 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