FDA-Device2020-03-18Class II
Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Cordis Corporation
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.
Sold states
US and UK
Affected count
89 units
Manufactured in
14201 NW 60th Ave, Miami Lakes, FL, United States
Products
Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1477-2020Don't want to check this manually?
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