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Endologix Lifts Hold On Shipments Of AAA Devices

 
• By Reed Miller

The Dec. 29 announcement relating to non-EU shipments of AFX and some AFX2 AAA repair devices came two days after the company said it suspended shipments of its flagship system because a manufacturing issue was causing damage to some devices. The release of the hold allowed the company to end a difficult month on a positive note. Endologix announced the suspension of the CE mark for AFX and AFX2 in Europe earlier in December.

Endologix Inc. has resumed shipping all sizes of its AFX abdominal aortic aneurysm (AAA) endograft systems as well as some sizes of its AFX2 AAA system based on reassuring testing results, the Irvine, California company announced Dec. 30.

The company announced it was temporarily suspending shipments of these devices on Dec. 27 because internal testing showed that the manufacturing process for these AAA repair devices may be damaging...

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