Abbott Medical: Medical Device Recall in 2024 - (Recall #: Z-0491-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.
Product Description:

Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, Sterile

Product Classification:

Class II

Date Initiated: October 17, 2024
Date Posted: November 27, 2024
Recall Number: Z-0491-2025
Event ID: 95627
Reason for Recall:

A manufacturing error resulting in acceptance of valves with a leaflet deflection value that was outside of established specifications. This could potentially affect long-term durability of the impacted valve and/or cause potential valve failure.

Status: Ongoing
Product Quantity: 1 US, 9 OUS
Code Information:

UDI-DI (GTIN): 05415067045768, Serial Numbers: 20078589, 20357219, 20357226, 20357685, 20358319, 20358343, 20358351, 20358363, 20358368, & 20358370.

Distribution Pattern:

New York, Australia, Belgium, Germany, Iran, Israel, Japan, Kazakhstan, Oman, Poland, Romania, Slovakia, Spain, Turkey, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated