Boston Scientific Corporation: Medical Device Recall in 2021 - (Recall #: Z-1591-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusions in the venous vasculature.

Product Classification:

Class I

Date Initiated: April 12, 2021

Date Posted: May 26, 2021

Recall Number: Z-1591-2021

Event ID: 87721

Reason for Recall:

The firm has received reports of stent migration after implantation

Status: Ongoing

Product Quantity: 550 units

Code Information:

all batches/lots of the device manufactured between May 2018 through April 2021

Distribution Pattern:

Worldwide - US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated