Medtronic Heart Valves, Inc.
FDA adverse event reports naming Medtronic Heart Valves, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC HEART VALVES, INC..
- Total reports
- 1,366
- Deaths
- 113
- Injuries
- 947
- Malfunctions
- 304
Reports per year
11000
9601
7402
6403
9304
2905
1806
11107
8908
11009
13510
12111
512
513
314
Source: FDA adverse event reports by year received, 2000–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Heart-Valve, Non-Allograft TissueLWR980
- Heart-Valve, MechanicalLWQ105
- Replacement Heart-ValveDYE66
- Pulmonic Valved ConduitMWH66
- Pulmonary Valve Prosthesis Percutaneously DeliveredNPV61
- Ring, AnnuloplastyKRH39
- Instruments, Surgical, CardiovascularDWS25
- Electrode, Pacemaker, TemporaryLDF13
- Sizer, Heart-Valve, ProsthesisDTI4
- Vessel Guard Or Cover, To Facilitate Revision SurgeriesMFX3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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