Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Syntel Silicone Thrombectomy Catheter Recalled by LeMaitre Vascular, Inc. Due to The guide tip can become damaged and result...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact LeMaitre Vascular, Inc. directly.
Affected Products
Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies.
Quantity: 5,604 units
Why Was This Recalled?
The guide tip can become damaged and result in the tip detaching.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About LeMaitre Vascular, Inc.
LeMaitre Vascular, Inc. has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report