🔍 RecallPedia

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

Class I - Dangerous
🏥 Medical Devices Recalled: May 16, 2025 Drs Vascular Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Drs Vascular, Inc
Reason for Recall:
XXX
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2330-2025