Boston Scientific Corporation VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusions in the venous vasculature. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusions in the venous vasculature.
Brand
Boston Scientific Corporation
Lot Codes / Batch Numbers
all batches/lots of the device manufactured between May 2018 through April 2021
Products Sold
all batches/lots of the device manufactured between May 2018 through April 2021
Boston Scientific Corporation is recalling VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusion due to The firm has received reports of stent migration after implantation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm has received reports of stent migration after implantation
Recommended Action
Per FDA guidance
Boston Scientific initiated the recall by letter on April 12, 2021. The letter requested the consignee cease use and further distribution of the affected product, segregate and return to Boston Scientific. Distributors were directed to further distribute the notice to their customers. For questions contact your local Sales Representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026