Class II — Drs Vascular, Inc
| Recalling firm | DRS VASCULAR, INC. |
|---|---|
| Registered facility | DRS VASCULAR, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | XXX |
| 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 assist with venous access hemostasis. Component: No |
| Quantity | 264 |
| Distribution | U.S. Nationwide distribution in the states of AR, CA, and NY. |
| Initiated | 2025-05-16 |
| Classified | 2025-08-15 |
| Recall number | Z-2330-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Drs Vascular, Inc (Z-2330-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97128/
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