Cordis Corporation recalls Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indi
Recalled Product
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Hazard / Issue
The product in the packaging is larger (both inner and outer diameter) than the labeling indicates.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Catalog: 504-657A Lot 17919780: Exp. Date 12/31/2022 and Lot 17988227: Exp. Date 10/31/2023
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