Recall Z-2330-2025— Drs Vascular, Inc
Class II · Ongoing
Class II FDA medical device recall by Drs Vascular, Inc, initiated 2025-05-16. FDA's recall record names no specific 510(k) clearance for this event. 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. Reason: XXX.
- Recalling firm
- Drs Vascular, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-05-16
- Firm location
- San Jose, CA, United States
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.