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
- 3,080
- Deaths
- 1
- Injuries
- 71
- Malfunctions
- 2,644
Reports per year
4297
3798
4499
2600
1001
4002
1103
3504
4005
8006
64707
43508
79109
60510
22011
Source: FDA adverse event reports by year received, 1997–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE1,974
- Calibrator, Multi-Analyte MixtureJIX304
- Immunoassay Method, Troponin SubunitMMI78
- Bromcresol Green Dye-Binding, AlbuminCIX73
- System, Test, Human Chorionic GonadotropinDHA59
- Visual, Pregnancy Hcg, Prescription UseJHI56
- Phosphomolybdate (Colorimetric), Inorganic PhosphorusCEO46
- Enzyme Linked Immunoabsorbent Assay, Toxoplasma GondiiLGD42
- Nad Reduction/Nadh Oxidation, Cpk Or IsoenzymesCGS36
- Station, Pipetting And Diluting, For Clinical UseJQW36
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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