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Cordis Corporation recalls Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Recalled November 6, 2019 · FDA recall Z-0250-2020 · Cordis
Hazard
Product was manufactured utilizing an expired inner body. · FDA Class II
Units
21 units
Sold at
US distribution to AL, AZ, FL, MN, and MO
Description
Product was manufactured utilizing an expired inner body.
Product
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Manufacturer(s)
Cordis Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →