Conmed Corp.
FDA adverse event reports naming Conmed Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: CONMED CORP..
- Total reports
- 1,132
- Deaths
- 10
- Injuries
- 219
- Malfunctions
- 650
Reports per year
710
411
312
413
314
1015
916
517
218
119
321
122
223
124
225
Source: FDA adverse event reports by year received, 2010–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI673
- Laparoscope, General & Plastic SurgeryGCJ87
- Applier, Surgical, ClipGDO58
- Electrode, ElectrocardiographDRX54
- Cannula, Manipulator/Injector, UterineLKF28
- Clip, ImplantableFZP22
- Electrode, CutaneousGXY22
- Applier, Hemostatic ClipHBT21
- Electrosurgical Patient Return ElectrodeODR17
- Electrode, ElectrosurgicalJOS16
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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