Device recall
Z-0015-2021: Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30" V-20…
FDA device recall · Class II · Riverpoint Medical, LLC
Key facts
| Recall number (Z-number) | Z-0015-2021 |
|---|---|
| Recall event | 86254 |
| Product | Velosorb Fast Braided Absorbable Suture: Covidien Velosorb 2/0 Undyed 30" V-20 Taper, Product Number: CV417G, UDI: 20884521149370 - Product Usage: indicated for use in soft tissue approximation of the skin and mucosa, where only 7-10 days of wound support is required, but not for use in ligation… |
| Product code | GAM |
| Recalling firm | Riverpoint Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 8, 2022 |
| 510(k) numbers | K120556 |
| FEI number | 3006981798 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 Products in the same recall event
- 100–999 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