Olympus Medical Systems Corp. Hinode Plant
FDA adverse event reports naming Olympus Medical Systems Corp. Hinode Plant as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OLYMPUS MEDICAL SYSTEMS CORP. HINODE PLANT.
- Total reports
- 1,170
- Deaths
- 0
- Injuries
- 526
- Malfunctions
- 644
Reports per year
320
6621
19422
29523
23924
22125
15226
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Duodenoscope And Accessories, Flexible/RigidFDT846
- Bronchoscope (Flexible Or Rigid)EOQ250
- Endoscope, Accessories, Narrow Band SpectrumNWB14
- Endoscopic Access Overtube, Gastroenterology-UrologyFED11
- Ultrasound BronchoscopePSV10
- Gastroscope And Accessories, Flexible/RigidFDS7
- Endoscopic Ultrasound System, Gastroenterology-UrologyODG7
- Cystoscope And Accessories, Flexible/RigidFAJ6
- Nasopharyngoscope (Flexible Or Rigid)EOB3
- Biopsy NeedleFCG2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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