Device recall
Z-2330-2025: Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number…
FDA device recall · Class II · Drs Vascular, Inc
Key facts
| Recall number (Z-number) | Z-2330-2025 |
|---|---|
| Recall event | 97128 |
| Product | Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Description: The DRS Vascular Q-Stop Suture Retention Appliance is a sterile, single-use, lightweight device made of biocompatible materials that can be easily installed within minutes to… |
| Product code | KGS |
| Recalling firm | Drs Vascular, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3030564133 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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