Z-2330-2025 Class II Ongoing
FDA device recall Z-2330-2025 was initiated by Drs Vascular, Inc on May 16, 2025 and is designated Class II. Reason for recall: XXX The recall status is ongoing. Affected quantity: 264.
Recall Details
- Product Type
- Devices
- Report Date
- August 27, 2025
- Initiation Date
- May 16, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 264
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
Reason for Recall
XXX
Distribution Pattern
U.S. Nationwide distribution in the states of AR, CA, and NY.
Code Information
Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402