FDAMay 6, 2020device

Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J

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

The hazard

A material weakness adjacent to the polymer fill channel may become compromised during pressurization with liquid polymer. Polymer leaks may occur during implantation of abdominal stent graft system. Clinical events related to polymer leaks may be systemic and/or aneurysm related.

What to do

FDA enforcement status: Terminated

Brands named

endologix

Recall history

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

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