FDA recall Z-0495-2025

Abbott Medical · Class II · device

Product

Abbott Navitor Transcatheter Aortic Heart Valve, 27 mm, NVTR-27, Sterile

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.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2024-10-17
Report date
2024-11-27
Voluntary/Mandated
Voluntary: Firm initiated
Location
Saint Paul, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0495-2025