Cordis Corporation recalls Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular u
Recalled Product
Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.
Hazard / Issue
Product was manufactured utilizing an expired inner body.
Issued by
FDA
Affected States: AL, AZ, FL, MN, MO
Lot/Code Info: Catalog Number: 4171460S; Lot Number: 82169860; Expiry Date: 10/31/2020
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