Drs Vascular, Inc recalls Brand Name: Q-Stop Product Name: Suture Retention Device Model/Catalog Number: QS Software Version: N/A Product Descrip…
- Recall date
- May 16, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2330-2025
- FDA classification
- Class II
- Brand / firm
- Drs Vascular, Inc
- Sold / distributed
- U.S. Nationwide distribution in the states of AR, CA, and NY.
Why it was recalled
XXX
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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
Get recall alerts
Free email alert whenever Drs Vascular, Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Drs Vascular, Inc