Every recall we track for Medtronic Vascular, Inc. — 11 in all — plus the complaints and injury reports the public filed about them.
Medtronic recalls specific IN.PACT Admiral balloon catheters due to potential packaging damage causing loss of sterility. Affected models include ADM04004013P and others listed. No remedy specified in recall notice.
Medtronic recalls Paclitaxel-coated PTA balloon catheters with packaging that may lose sterility, risking infection during procedures. Affected units include specific lot numbers and model codes.
Medtronic recalls Endurant, Endurant II, and Endurant IIs stent graft systems with specific batch numbers that may detach during implant, requiring removal or leaving behind in patients.
Medtronic recalls Endurant IIs Stent Graft System with serial numbers starting with ESBF2814C103EE due to potential spindle detachment during deployment, which could cause complications. Affected units include specific model numbers and serial ranges.
Medtronic recalls Endurant Stent Graft System model ENTF2525C70EE due to spindle detachment risk during deployment. Affected units have specific serial numbers and GTIN code.
Medtronic recalls Endurant II Stent Graft Systems with specific model numbers due to risk of spindle detaching during deployment, which could cause complications. Affected units include ETBF2513C145EE and other variants listed in the recall.
Medtronic recalls Endurant IIs Stent Graft Systems with specific model numbers due to risk of radiopaque marker detachment during deployment, potentially affecting aneurysm treatment procedures.
Medtronic recalls Endurant II stent graft systems with specific model numbers due to risk of radiopaque marker detaching during deployment, potentially causing complications.
Medtronic recalls Endurant II stent grafts with incorrect stentstop assembly (18fr) that could cause device malfunction during vascular aneurysm treatment.
Medtronic Vascular recalls Valiant Navion Thoracic Stent Graft System (models VNMC2020C94TE, VNMC2020C94TJ, etc.) for endoleaks, stent fractures, and stent ring enlargement. Affected patients should contact Medtronic for evaluation.
