Olympus Winter & Ibe Gmbh
FDA adverse event reports naming Olympus Winter & Ibe Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: Olympus Winter & Ibe GmbH.
- Total reports
- 1,354
- Deaths
- 0
- Injuries
- 6
- Malfunctions
- 1,348
Top device categories
- Laparoscope, Gynecologic (And Accessories)HET867
- Hysteroscope (And Accessories)HIH189
- Endoscope, RigidGCM91
- Endoscope, Accessories, Narrow Band SpectrumNWB86
- Nasopharyngoscope (Flexible Or Rigid)EOB21
- Cystoscope And Accessories, Flexible/RigidFAJ20
- Laparoscope, General & Plastic SurgeryGCJ12
- UrethroscopeFGC11
- Endoscope, Ac-Powered And AccessoriesGCP10
- Bronchoscope (Flexible Or Rigid)EOQ9
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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