Vascutek recalls

Vascutek appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2026-03-11.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE,…
  FDA Device · Class II · 2026-03-11 · Vascutek
• The Instructions for Use (IFU) for: Carotid Patch and Gelsoft Patch vascular patches
  FDA Device · Class II · 2021-10-06 · Vascutek
• The Instructions for Use (IFU) for: Gelsoft Plus Bifurcate, Gelsoft Plus Ax-Fem, GelsoftPlus ERS Ax-Fem, Gelweave Straight, Gelweave Trifur…
  FDA Device · Class II · 2021-10-06 · Vascutek
• Gelseal Straight Diameter 8mm Length 30cm
  FDA Device · Class II · 2015-07-08 · Vascutek
• Gelseal Straight Diameter 8mm Length 15cm
  FDA Device · Class II · 2015-07-08 · Vascutek
• Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company
  FDA Device · Class II · 2014-08-27 · Vascutek