Siemens Healthcare Diagnostics Inc - Glasgow
FDA adverse event reports naming Siemens Healthcare Diagnostics Inc - Glasgow as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW.
- Total reports
- 2,004
- Deaths
- 1
- Injuries
- 5
- Malfunctions
- 1,981
Reports per year
1110
18511
37212
36113
36814
21315
35416
14017
Source: FDA adverse event reports by year received, 2010–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Immunoassay Method, Troponin SubunitMMI480
- Assay, Glycosylated HemoglobinLCP316
- Urease And Glutamic Dehydrogenase, Urea NitrogenCDQ230
- Electrode, Ion Specific, SodiumJGS228
- Calibrator, SecondaryJIT60
- Enzymatic Method, CreatinineJFY58
- Radioimmunoassay, Thyroid-Stimulating HormoneJLW57
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE50
- Cresolphthalein Complexone, CalciumCIC48
- Fibrinogen And Fibrin Split Products, Antigen, Antiserum, ControlDAP39
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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