Class II

Medical Device Recall: Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies.

LeMaitre Vascular, Inc. · April 17, 2024

Reason for Recall

The guide tip can become damaged and result in the tip detaching.

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Canada, and Spain.

States Affected

NATIONWIDE

Quantity Affected

5,604 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1824-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

LeMaitre Vascular, Inc. Medical Device Recall: Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies. | SafeCheck