Toronto, N/A, Canada
Conavi Medical Inc. recalls
1 recall recorded since 2018, most recently on 12 March 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)1
Ongoing Class I Medical devices
- Recall started
- 12 March 2025
- Reason
- Due to manufacturing issues there is a potential for the catheter sheath to detach.
- Distribution
- US distribution to states of: GA, NY, NJ, OH; and OUS (Foreign) to countries of: Canada and China
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1585-2025
- Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product Description: Common Name: Diagnostic intravascular catheter Description: The Novasight Hybrid cathe
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.