Device recall
Z-2030-2010: Medtronic U-CLIP Double Arm Approximation Device, model V100D U-Clip, Catalog…
FDA device recall · Class II · Medtronic Cardiovascular Revascularization & Surgical Therap
Key facts
| Recall number (Z-number) | Z-2030-2010 |
|---|---|
| Recall event | 55900 |
| Product | Medtronic U-CLIP Double Arm Approximation Device, model V100D U-Clip, Catalog Number V100DRFRN2. Sterilized using Irradiation. The U-Clip consists of specially designed vascular clips optionally connected to needles via flexible members. These clips may or may not include coils surrounding a Nitinol… |
| Product code | FZP |
| Recalling firm | Medtronic Cardiovascular Revascularization & Surgical Therap |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2011 |
| 510(k) numbers | K031623 |
| FEI number | 1000116158 |
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