Plexus Manufacturing SDN. BHD
FDA adverse event reports naming Plexus Manufacturing SDN. BHD as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PLEXUS MANUFACTURING SDN. BHD.
- Total reports
- 5,574
- Deaths
- 8
- Injuries
- 374
- Malfunctions
- 5,192
Reports per year
2711
2512
1313
7614
43315
57216
81817
1,19518
1,34919
1,06120
521
Source: FDA adverse event reports by year received, 2011–2021. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pulse-Generator, Pacemaker, ExternalDTE3,966
- Pulse Generator, Permanent, ImplantableNVZ558
- Programmer, PacemakerKRG523
- Analyzer, Pacemaker Generator FunctionDTC238
- Stimulator, Electrical, Implantable, For IncontinenceEZW167
- Pacemaker/Icd/Crt Non-Implanted ComponentsOSR48
- Implantable Pulse Generator, Pacemaker (Non-Crt)LWP31
- Detector And Alarm, ArrhythmiaDSI23
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW10
- Cardiac Ablation Percutaneous CatheterLPB5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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