Medtronic Vascular recalls

Medtronic Vascular has 227 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 18 May 2022. 7 are still ongoing.

Total recalls227since 2013
Last 12 months0reported
Class I20389% of total
Ongoing7latest 18 May 2022

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 203 89%Class II 22 10%Class III 2 1%

Why medtronic vascular is recalled

By year

Ongoing medtronic vascular recalls

7 active

All medtronic vascular recalls, newest first

227 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIMedtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon recalledMedtronic VascularSterilityNationwide
DeviceCLASS IIMedtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter recalledMedtronic VascularSterilityNationwide
DeviceCLASS IIEndurant IIs Stent Graft System recalled by Medtronic VascularMedtronic VascularOtherNationwide
DeviceCLASS IIEndurant Stent Graft System recalled by Medtronic VascularMedtronic VascularOtherNationwide
DeviceCLASS IIEndurant II Stent Graft System recalled by Medtronic VascularMedtronic VascularOtherNationwide
DeviceCLASS IIMedtronic Endurant IIs Stent Graft System Medtronic recalledMedtronic VascularOther8 states
DeviceCLASS IIEndurant II/Endurant IIs Stent Graft System recalledMedtronic VascularOther8 states
DeviceCLASS IIEndurant II/IIs Stent Graft System recalled by Medtronic VascularMedtronic VascularOtherNationwide
DeviceCLASS IAngiographic Guidewire Component recalled by Medtronic VascularMedtronic VascularOther11 states
DeviceCLASS IIMedtronic 6F Launcher Guide Catheter 100 cmJL recalledMedtronic VascularSterilityNationwide
DeviceCLASS IIMedtronic 6F Launcher Guide Catheter JR recalled by Medtronic VascularMedtronic VascularSterilityNationwide
DeviceCLASS IIMedtronic 6F Launcher Guide Catheter EBU recalled by Medtronic VascularMedtronic VascularSterilityNationwide
DeviceCLASS IIMedtronic 6F Launcher Guide Catheter EBU recalled by Medtronic VascularMedtronic VascularSterilityNationwide
DeviceCLASS IRashkind Balloon Septostomy Catheter, 5F, Closed end recalledMedtronic VascularDevice MalfunctionNationwide
DeviceCLASS IRashkind Balloon Septostomy Catheter, 4F, Closed end recalledMedtronic VascularDevice MalfunctionNationwide
DeviceCLASS IRashkind Balloon Septostomy Catheter, 6F, Recess Balloon recalledMedtronic VascularDevice MalfunctionNationwide
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Ar2.0070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Rcb Sh, 070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Lcb Sh, .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Mp St, .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Ar1.0sh070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Jl4.5, .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Ar1.0070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Al1.0 .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Noto, 070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Rbu4.0 Sh, .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Rbu3.5, 070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Erad Left Sh, .070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f, Hsi, 070" recalledMedtronic VascularOtherMA
DeviceCLASS ISherpa Nx Active Guiding Catheter, 6f Sal3.0, .070" recalledMedtronic VascularOtherMA

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.