Home / Recalls / Medical Devices
Cordis Corporation recalls Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Recalled March 18, 2020 · FDA recall Z-1477-2020 · Cordis
Hazard
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. · FDA Class II
Units
89 units
Sold at
US and UK
Description
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.
Product
Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Manufacturer(s)
Cordis Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →