medical Class II Updated 2020-03-18

Cordis Corporation recalls Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S

Recalled Product

Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S

Hazard / Issue

Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to the potential for body/shaft voids in the proximal seal area.

Issued by

FDA

Distribution: US and UK
Lot/Code Info: Lot 82155955, Use by date 2021-06-30
View official government recall

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