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
- 4,657
- Deaths
- 37
- Injuries
- 392
- Malfunctions
- 4,212
Reports per year
1505
906
1207
1308
3109
32510
1,94611
1,90612
4213
6914
12215
4516
617
418
122
Source: FDA adverse event reports by year received, 2005–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pulse-Generator, Pacemaker, ExternalDTE3,541
- Pulse Generator, Permanent, ImplantableNVZ467
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP290
- Implantable Pacemaker Pulse-GeneratorDXY189
- Detector And Alarm, ArrhythmiaDSI66
- Programmer, PacemakerKRG41
- Cardiac Ablation Percutaneous CatheterLPB24
- Implantable Cardioverter Defibrillator (Non-Crt)LWS12
- ElectrocardiographDPS10
- Permanent Pacemaker ElectrodeDTB7
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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