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Boston Scientific Corporation recalls VICI RDS VENOUS STENT System Product Usage: is indicated for improving luminal diameter in the iliofemoral veins for
Recalled May 26, 2021 · FDA recall Z-1592-2021 · Boston Scientific
Hazard
The firm has received reports of stent migration after implantation · FDA Class I
Units
34,248 units
Sold at
Worldwide - US Nationwide Distribution
Description
The firm has received reports of stent migration after implantation
Product
VICI RDS VENOUS STENT System Product Usage: is indicated for improving luminal diameter in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
Manufacturer(s)
Boston Scientific Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →