Drs Vascular, Inc: Device Recall
Recall #Z-2330-2025 · 05/16/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2330-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Drs Vascular, Inc
- Status
- Ongoing
- Date Initiated
- 05/16/2025
- Location
- San Jose, CA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 264
Reason for Recall
XXX
Product 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
Distribution Pattern
U.S. Nationwide distribution in the states of AR, CA, and NY.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.