San Jose, CA, United States
Drs Vascular, Inc recalls
1 recall recorded since 2018, most recently on 16 May 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 16 May 2025
- Reason
- XXX
- Distribution
- U.S. Nationwide distribution in the states of AR, CA, and NY.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2330-2025
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.