Device recall
Z-0164-2011: LeMaitre Vascular AnastoClip GC Vessel Closure System-Medium Size Models…
FDA device recall · Class III · Lemaitre Vascular, Inc.
Key facts
| Recall number (Z-number) | Z-0164-2011 |
|---|---|
| Recall event | 56908 |
| Product | LeMaitre Vascular AnastoClip GC Vessel Closure System-Medium Size Models: 4007-02 Medium size 3 Pack 4008-02 Medium size 10 Pack 4007-06 Medium size 1 Pack Manufactured by LeMatire Vascular Inc, Burlington, MA 01803 |
| Product code | HBT |
| Recalling firm | Lemaitre Vascular, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 15, 2011 |
| 510(k) numbers | K091987 |
| 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