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
This recall is currently active, issued August 15, 2025. It was issued by Drs Vascular, Inc.
- Company
- Drs Vascular, Inc
- Recall Initiated
- May 16, 2025
- Posted
- August 15, 2025
- Recall Number
- Z-2330-2025
- Quantity
- 264
- Firm Location
- San Jose, CA
- Official Source
- View on FDA website ↗
Reason for Recall
XXX
Distribution
U.S. Nationwide distribution in the states of AR, CA, and NY.
Lot / Code Info
Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402
Root Cause
Device Design
Action Taken
On 05/29/2025, the firm sent via FedEx next day an "URGENT MEDICAL DEVICE RECALL" Letter to customers informing them that they are conducting a voluntary recall of the Q-Stop Suture Retention Device Model QS due to some devices are prone to premature cutting of the suture. Customers are instructed to return all Q-Strop Suture Retention Device. Any used devices should be sent back in a sealed container. For questions contact firm at 510-345-7233 or mtaimisto@drsvascular.com