FDA recall Z-1585-2025

Conavi Medical Inc. · Class I · device

Product

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 catheter is a 3Fr single use, sterile device, which will be able to perform transluminal ultrasound and optical coherence tomography imaging of adults. The catheter is capable of real-time 2D side viewing ultrasound and optical imaging acquired simultaneously providing precisely co-registered images with the ability to produce rapidly post processed rendered longitudinal images of the vessel. Packaging: The Novasight Hybrid Catheter is packaged in a packaging system including the protective packaging and the sterile barrier system.

Reason for recall

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

Key facts

Status
Ongoing
Initiation date
2025-03-12
Report date
2025-04-30
Voluntary/Mandated
Voluntary: Firm initiated
Location
Toronto, N/A, Canada

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1585-2025