Q-Stop Suture Device (Drs Vascular) – Unknown Issue (2025)
This recall may present a risk under certain conditions.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
Drs Vascular, Inc
Lot Codes / Batch Numbers
Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402
Products Sold
Lot Code: 00860011629405 (6-pack) Unit of use: 10860011629402
Drs Vascular, Inc is recalling Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: due to XXX. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
XXX
Recommended Action
Per FDA guidance
On 05/29/2025, the firm sent via FedEx next day an "URGENT MEDICAL DEVICE RECALL" Letter to customers informing them that they are conducting a voluntary recall of the Q-Stop Suture Retention Device Model QS due to some devices are prone to premature cutting of the suture. Customers are instructed to return all Q-Strop Suture Retention Device. Any used devices should be sent back in a sealed container. For questions contact firm at 510-345-7233 or mtaimisto@drsvascular.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026