Olympus Medical Systems Corporation
FDA adverse event reports naming Olympus Medical Systems Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OLYMPUS MEDICAL SYSTEMS CORPORATION.
- Total reports
- 3,455
- Deaths
- 35
- Injuries
- 434
- Malfunctions
- 2,652
Reports per year
20808
25109
18910
19811
35012
55513
1,00514
50215
6016
2117
118
1519
920
1621
122
Source: FDA adverse event reports by year received, 2008–2022. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI963
- Instrument, Ultrasonic SurgicalLFL618
- Colonoscope And Accessories, Flexible/RigidFDF323
- Bronchoscope (Flexible Or Rigid)EOQ183
- Duodenoscope And Accessories, Flexible/RigidFDT137
- Gastroscope And Accessories, Flexible/RigidFDS119
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS119
- Product code KOGKOG114
- Lithotriptor, Biliary MechanicalLQC66
- Light Source, Endoscope, Xenon ArcGCT55
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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