Dublin, Ireland-based Covidien has issued a voluntary recall of certain lots of its Pipeline Embolization Device and Alligator Retrieval Device due to the potential for the polytetrafluoroethylene ...

DUBLIN, Ireland--(BUSINESS WIRE)--Covidien plc today announced that it has notified customers of a voluntary recall to address an issue with certain lots of its Pipeline™ Embolization Device and ...

Medtronic Plc (NYSE: MDT) is recalling its Pipeline Flex Embolization Device and Pipeline Flex Embolization Device with Shield Technology stents due to a risk of the devices' wires and tubes ...

The U.S. FDA has posted several class I recalls in recent days, including a removal of one model of the Medtronic Vascular’s Pipeline Vantage embolization device due to insufficient apposition to the ...

This voluntary recall is being conducted due to the potential separation and detachment of the polytetrafluoroethylene (PTFE) coating on parts of these devices. Should the PTFE separate from the ...