Recall
FDAHealthMay 16, 2025

Drs Vascular, Inc — 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

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Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 16, 2025

U.S. Nationwide distribution in the states of AR, CA, and NY.

What's affected?

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
Lot code
00860011629405

Additional details

Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 264.

View original FDA notice →

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