AllClear
PricingSign in
FDADecember 27, 2016device

AFX Endovascular AAA System, Endoleak Type IIIA

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

The hazard

Endologix initiated a correction by updating reports for the cumulative clinical data and information on the Powerlink System and the AFX Endovascular AAA System (AFX System).

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.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →