RecallDepth

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