Olympus Winter & IBE Gmbh Berlin Facility
FDA adverse event reports naming Olympus Winter & IBE Gmbh Berlin Facility as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: OLYMPUS WINTER & IBE GMBH BERLIN FACILITY.
- Total reports
- 2,045
- Deaths
- 2
- Injuries
- 132
- Malfunctions
- 1,911
Reports per year
4822
36523
57524
67325
38426
Source: FDA adverse event reports by year received, 2022–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI2,033
- Generator, Low Voltage, Therapeutic X-RayIYD4
- Electrode, Electrosurgical, Active, UrologicalFAS3
- Pump, Air, Non-Manual, For EndoscopeFEQ1
- Colonoscope, General & Plastic SurgeryFTJ1
- Curette, Suction, Endometrial (And Accessories)HHK1
- Hysteroscope (And Accessories)HIH1
- Generator, High-Voltage, X-Ray, DiagnosticIZO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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