Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1824-2024 — Syntel Silicone Thrombectomy Catheter, Sterile, Rx Only. Used in vascular grafts and peripheral venous thrombectomies.

U.S. FDA — Device Enforcement · United States · 2024-04-17 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1824-2024
Date of alert
2024-04-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
LeMaitre Vascular, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
840663109807
Reported risk: The guide tip can become damaged and result in the tip detaching.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.