Device recall
Z-2513-2023: Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring…
FDA device recall · Class II · Cook Vandergrift, Inc.
Key facts
| Recall number (Z-number) | Z-2513-2023 |
|---|---|
| Recall event | 92791 |
| Product | Cook Lead Clipper- An auxiliary tool indicated for use in patients requiring percutaneous retrieval of cardiac leads. Order Number (GPN): G20003 Reference Part Number (RPN): LR-CLP001 |
| Product code | DWS |
| Recalling firm | Cook Vandergrift, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2522007 |
At a glance
- None 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