FDAFebruary 11, 2020device

Medtronic Open Pivot Aortic Valve Graft, REF 502AG25, SIZE 25 mm

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Medtronic received a complaint from China that the label on the box for an Open Pivot Heart Valve was labeled as Aortic, but the product was Mitral. The valve itself was correctly labeled as Mitral.

What to do

FDA enforcement status: Terminated

Brands named

medtronic ats medicalmedtronicmedtronic ats

UPCs

00643169297913

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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