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FDA (Device enforcement)Recalled 2024-10-17class ii

Abbott Medical: Abbott Navitor Transcatheter Aortic Heart Valve, 29 mm, NVTR-29, Sterile

Hazard

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.

Details from the source

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. Quantity: 1 OUS Lot/code info: UDI-DI (GTIN): 5415067031600, Serial Number: 20131478

UPC codes

5415067031600

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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