Microvention Inc.

Microvention Inc.: 2 recalls posted by FDA since May 2026.

By agency

FDA2

By category

Medical Device2

By hazard

Device defect2

All recalls (2)

BOBBY Balloon Guide Catheter

The BOBBY Balloon Guide Catheter has an increased rate of balloon pinhole defects.

Moderate riskFDAAug 7, 2026Device defect

LVIS Intraluminal Support Device

The LVIS Intraluminal Support Device may have dimensional nonconformance or incorrect configuration, potentially causing vessel injury or neurological events.

Moderate riskFDAMay 14, 2026Device defect

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