Abbott Manufacturing Inc
FDA adverse event reports naming Abbott Manufacturing Inc as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABBOTT MANUFACTURING INC.
- Total reports
- 5,511
- Deaths
- 6
- Injuries
- 112
- Malfunctions
- 5,378
Reports per year
105
306
707
1208
410
30111
51912
36813
26014
30515
28116
39117
2,18918
78119
8120
Source: FDA adverse event reports by year received, 2005–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE2,712
- Nad Reduction/Nadh Oxidation, Cpk Or IsoenzymesCGS1,440
- Calculator/Data Processing Module, For Clinical UseJQP436
- Photometric Method, MagnesiumJGJ94
- Electrode, Ion Specific, SodiumJGS90
- Azo Dye, CalciumCJY74
- Immunoassay Method, Troponin SubunitMMI70
- Urease And Glutamic Dehydrogenase, Urea NitrogenCDQ69
- Alkaline Picrate, Colorimetry, CreatinineCGX58
- Test, Equipment, Automated Bloodborne PathogenMZA46
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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