Z-0495-2025 Class II Ongoing

Recalled by Abbott Medical — Saint Paul, MN

Recall Details

Product Type
Devices
Report Date
November 27, 2024
Initiation Date
October 17, 2024
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
5 OUS

Product Description

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 Pattern

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

Code Information

UDI-DI (GTIN): 5415067031594, Serial Numbers: 20110016, 20155472, 20155476, 20166304, & 20168050.