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Recall Observatory FDA recall evidence

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.

Z-1585-2025

March 12, 2025

Class I

Product summary

Firm
Conavi Medical Inc.
Event
Event 96444
Status
Ongoing
Classification
Class I
Quantity
685
Official record key
device-enforcement:Z-1585-2025

Official wording

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

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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