Device recall
Z-3042-2018: AnastoClip GC Closure System, REF# 4007-08 a closure system designed to…
FDA device recall · Class II · LeMaitre Vascular, Inc.
Key facts
| Recall number (Z-number) | Z-3042-2018 |
|---|---|
| Recall event | 80627 |
| Product | AnastoClip GC Closure System, REF# 4007-08 a closure system designed to penetrate the outer layers of tissue during the forming of an anastomosis or closing of a vessel with possible intraluminal penetration. |
| Product code | HBT |
| Recalling firm | LeMaitre Vascular, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 17, 2019 |
| 510(k) numbers | K173323 |
| FEI number | 1220948 |
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