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Cordis Corporation recalls Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring pe
Recalled July 21, 2021 · FDA recall Z-2079-2021 · Cordis
Hazard
The product in the packaging is larger (both inner and outer diameter) than the labeling indicates. · FDA Class II
Units
680 units
Sold at
Worldwide distribution - US Nationwide distribution in the states of AR, AZ, FL, GA, IN, NC, NJ, and WV. The country of Canada.
Description
The product in the packaging is larger (both inner and outer diameter) than the labeling indicates.
Product
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduction of intravascular devices.
Manufacturer(s)
Cordis Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →