Bio-rad Medical Diagnostics Gmbh
FDA adverse event reports naming Bio-rad Medical Diagnostics Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BIO-RAD MEDICAL DIAGNOSTICS GMBH.
- Total reports
- 1,480
- Deaths
- 2
- Injuries
- 1
- Malfunctions
- 1,475
Reports per year
20912
11813
7914
5715
9816
10517
9218
8019
10020
9121
7422
6423
4724
3425
1626
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Test, Automated Blood Grouping And AntibodyKSZ1,069
- Blood Grouping ReagentQHR223
- Reagent Red Blood CellsQHT101
- Anti-Human GlobulinQHS27
- Kit, Quality Control For Blood Banking ReagentsKSF21
- Antinuclear Antibody, Antigen, ControlLKJ19
- Igg, Antigen, Antiserum, ControlDEW14
- System, Image Processing, RadiologicalLLZ2
- Acid, Folic, RadioimmunoassayCGN1
- Anti-Human Globulin, Fta-Abs TestGMS1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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