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Recall Observatory FDA recall evidence

Device product

Abbot Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 29 mm, NVRO-29, Sterile

Z-0493-2025

October 17, 2024

Class II

Product summary

Firm
Abbott Medical
Event
Event 95627
Status
Ongoing
Classification
Class II
Quantity
3 OUS
Official record key
device-enforcement:Z-0493-2025

Official wording

Reason: 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.

Code information: UDI-DI (GTIN): 5415067045775, Serial Numbers: 20150441, 20156804, & 20170535

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

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing error