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LeMaitre Vascular, Inc.

LeMaitre Vascular, Inc.: 2 recalls listed since March 2026 across FDA.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

LeMaitre Vascular TufTex Over-the-Wire Embolectomy Catheter

The TufTex Over-the-Wire Embolectomy Catheter can fail under pull force, causing balloon components to fail.

Moderate risk, FDA, , Device defect

Artegraft Vascular Graft

The Artegraft Vascular Graft has a labeling mix-up resulting in incorrect lot outer packaging.

Moderate risk, FDA, , Labeling error
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