Hamilton Bonaduz Ag
FDA adverse event reports naming Hamilton Bonaduz Ag as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: HAMILTON BONADUZ AG.
- Total reports
- 4,327
- Deaths
- 0
- Injuries
- 0
- Malfunctions
- 3,020
Reports per year
20500
14701
3802
2103
27004
45005
45206
57507
44008
27809
17610
19511
22612
31013
314
Source: FDA adverse event reports by year received, 2000–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Device, Microtiter Diluting/DispensingJTC3,571
- Blood Establishment Computer Software And AccessoriesMMH691
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE46
- Plasma, Coagulase, Human, Horse And RabbitJTL9
- Station, Pipetting And Diluting, For Clinical UseJQW7
- Product code ------3
- Pipette, Quantitative, HematologyGJG3
- Bath, Incubators/Water, AllJTQ1
- System, Test, Automated Blood Grouping And AntibodyKSZ1
- Instrument For Auto Reader Of Overnight Microorganism Identification SystemLRH1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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