Medtronic AVE Peripheral Division
FDA adverse event reports naming Medtronic AVE Peripheral Division as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC AVE PERIPHERAL DIVISION.
- Total reports
- 1,183
- Deaths
- 124
- Injuries
- 858
- Malfunctions
- 175
Reports per year
299
6200
29601
26902
29003
26304
105
Source: FDA adverse event reports by year received, 1999–2005. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Endovascular Graft, Aortic Aneurysm TreatmentMIH1,048
- Stents, Drains And Dilators For The Biliary DuctsFGE124
- Stent, CoronaryMAF5
- Shunt, Portosystemic, EndoprosthesisMIR2
- Product code ------1
- System, Balloon, Intra-Aortic And ControlDSP1
- Prosthesis, Vascular Graft, Of 6mm And Greater DiameterDSY1
- Stent, RenalNIN1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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