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Conavi Medical Inc. recalls Brand Name: Novasight Hybrid System Product Name: Novasight Hybrid Catheter Model/Catalog Number: TA-06-0001 Product
Recalled April 30, 2025 · FDA recall Z-1585-2025 · Conavi Medical
Hazard
Due to manufacturing issues there is a potential for the catheter sheath to detach. · FDA Class I
Units
685
Sold at
US distribution to states of: GA, NY, NJ, OH; and OUS (Foreign) to countries of: Canada and China
Description
Due to manufacturing issues there is a potential for the catheter sheath to detach.
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.
Manufacturer(s)
Conavi Medical Inc.
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →