Conavi Medical Inc.: Medical Device Recall in 2025 - (Recall #: Z-1585-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.
Product Description:

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.

Product Classification:

Class I

Date Initiated: March 12, 2025
Date Posted: April 30, 2025
Recall Number: Z-1585-2025
Event ID: 96444
Reason for Recall:

Due to manufacturing issues there is a potential for the catheter sheath to detach.

Status: Ongoing
Product Quantity: 685
Code Information:

Model No: TA-06-0001 UDI-DI: (01)00628055603054 Lot number: 230902; Expiration date: 2024-06; Lot number: 240202; Expiration date: 2025-03; Lot number: 240302; Expiration date: 2025-04; Lot number: 240402; Expiration date: 2025-05; Lot number: 240502; Expiration date: 2025-06; and all catheter lots which were expired (See attachment 2a, 2b and 2c for details).

Distribution Pattern:

US distribution to states of: GA, NY, NJ, OH; and OUS (Foreign) to countries of: Canada and China

Voluntary or Mandated:

Voluntary: Firm initiated