Medtronic Inc.
Plymouth, MN
This page shows every FDA and USDA recall linked to Medtronic 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.
7
Total Recalls
2017
First Recall
2026
Most Recent
Abre Venous Self-Expanding Stent System, Model numbers AB9G14120090
AB9G12100090
AB9G14080090
AB9G12080090
AB9...
Jan 15, 2026
· Device
Open, Classified
Abre Venous Self-expanding Stent System, Product Numbers:
a) AB9U14080090;
b) AB9U18100090;
c) AB9G1410009...
Mar 19, 2024
· Device
Open, Classified
Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.
Jan 2, 2024
· Device
Completed
EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System
Jul 14, 2022
· Device
Open, Classified
VenaSeal Closure System
Mar 23, 2021
· Device
Open, Classified
Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended fo...
Mar 16, 2021
· Device
Terminated
Everflex Self-Expanding Peripheral Stent with Entrust Delivery System
Intended to improve luminal diameter in...
Nov 3, 2017
· Device
Terminated