Medtronic Milaca, Inc.
FDA adverse event reports naming Medtronic Milaca, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MEDTRONIC MILACA, INC..
- Total reports
- 6,065
- Deaths
- 5
- Injuries
- 611
- Malfunctions
- 5,448
Reports per year
3811
18212
1,60413
1,36314
1,13115
33116
34617
24318
22419
14420
13621
13622
8523
6524
3225
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP5,607
- Pulse-Generator, Pacemaker, ExternalDTE226
- Pulse Generator, Permanent, ImplantableNVZ123
- Cardiac Ablation Percutaneous CatheterLPB38
- Programmer, PacemakerKRG34
- Implantable Pacemaker Pulse-GeneratorDXY21
- ElectrocardiographDPS6
- Pacemaker/Icd/Crt Non-Implanted ComponentsOSR4
- Detector And Alarm, ArrhythmiaDSI1
- Permanent Pacemaker ElectrodeDTB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Medtronic Milaca, Inc. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.