W. L. Gore & Associates Inc.
Phoenix, AZ
This page shows every FDA and USDA recall linked to W. L. Gore & Associates Inc.. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
4
Total Recalls
2019
First Recall
2021
Most Recent
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidew...
Jul 12, 2021
· Device
Open, Classified
GORE EXCLUDER Iliac Branch Endoprosthesis
(IBE)
Jan 6, 2020
· Device
Terminated
GORE EXCLUDER AAA Endoprosthesis
Jan 6, 2020
· Device
Terminated
Gore DrySeal Flex Introducer Sheath, Catalog #DSF1433, 33cm 14FR, Sterile. The responsible firm on the label...
Nov 18, 2019
· Device
Terminated