FDAJune 12, 2015device

On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions

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

The hazard

Incorrect product label. The type of Sewing Ring was mislabeled as being a Standard Sewing Ring instead of an Anatomic Sewing Ring.

What to do

FDA enforcement status: Terminated

Brands named

cryolife

Recall history

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

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