Medtronic Cardiovascular
Santa Rosa, CA
This page shows every FDA and USDA recall linked to Medtronic Cardiovascular. 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
2007
First Recall
2011
Most Recent
Pioneer Plus Catheter PPlus 120 dual lumen device, inserted through a 6F introducer sheath and placed percuta...
Jan 6, 2011
· Device
Terminated
Medtronic Racer Biliary Stent System, Model number XD518YF, UPC code 00721902758164 in a box containing steril...
Jun 14, 2010
· Device
Terminated
Complete SE Biliary Stent System, SC680L (6 mm x 120 mm), lot number 0000983806, UPC code 006133994186669, use...
Jan 19, 2010
· Device
Terminated
Complete SE Biliary Stent System, SC5120L (5 mm x 12 mm), lot number 0000983799, UPC code 00613994186478, use...
Jan 19, 2010
· Device
Terminated
Medtronic COMPLETE SE Self Expanding Biliary Stent System, Model number SC760L, includes a pre-loaded self-exp...
Mar 18, 2009
· Device
Terminated
AneuRx AAAdvantage stent graft and the Xcelerant Delivery System with Hydro, Product number ILXCH161685, manuf...
Sep 16, 2008
· Device
Terminated
Medtronic brand AneuRx AAAdvantage Endovascular Stent Graft with the Xcelerant Delivery System;
Model Numbe...
Apr 8, 2008
· Device
Terminated