FDAJanuary 4, 2017device

AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-02 BEA28-100/I20-40 F00820-03 BEA28-80/I20-40 F00820-06 BEA28-120/I16-40 F00820-07 BEA28-100/I16-40 F00820-08 BEA28-80/I16-40 F00820-09 BEA28-60/I16-40 F00820-16 BEA28-110/I20-30 F00820-17 BEA28-90/I20-30 F00...

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

The hazard

Endologix updated information on the rates of Type III endoleaks and suggestions for patient surveillance and treatment.

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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