Every recall we track for Endologix — 4 in all — plus the complaints and injury reports the public filed about them.
Endologix recalls specific AFX/AFX2 endograft models due to potential Type III endoleaks requiring enhanced patient surveillance. This follow-up notice addresses updated warnings for interventions involving these devices.
Endologix recalls AFX2 Bifurcated Endograft Systems for potential Type III endoleaks requiring additional monitoring after December 2016.
Endologix recalls specific AFX Endovascular AAA stent graft systems due to potential Type III endoleaks requiring additional monitoring. Patients should follow updated surveillance recommendations.
Endologix recalls specific AFX/AFX2 endograft models due to potential Type III endoleaks requiring patient surveillance. This follow-up notification addresses updated monitoring recommendations.
