Boston Scientific Corporation recalls VICI RDS VENOUS STENT System Product Usage: is indicated
Recalled 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.
Hazard / Issue
The firm has received reports of stent migration after implantation
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: all batches/lots of the device manufactured between May 2018 through April 2021
View official government recall
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