FDA-Device2019-11-06Class II
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Cordis Corporation
Hazard
Product was manufactured utilizing an expired inner body.
Sold states
US distribution to AL, AZ, FL, MN, and MO
Affected count
21 units
Manufactured in
14201 NW 60th Ave, Miami Lakes, FL, United States
Products
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0250-2020Don't want to check this manually?
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