Abbott Germany
FDA adverse event reports naming Abbott Germany as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABBOTT GERMANY.
- Total reports
- 2,710
- Deaths
- 0
- Injuries
- 73
- Malfunctions
- 2,637
Reports per year
108
3110
13311
17812
25113
19814
8015
10616
17117
56018
1,00119
Source: FDA adverse event reports by year received, 2008–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Analyzer, Chemistry (Photometric, Discrete), For Clinical UseJJE894
- Radioimmunoassay, Parathyroid HormoneCEW473
- Assay, Enzyme Linked Immunosorbent, Hepatitis C VirusMZO283
- Test, Hiv DetectionMZF209
- Hepatitis A Test (Antibody And Igm Antibody)LOL202
- Radioimmunoassay, VancomycinLEH130
- Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)LOM111
- System, Test, Carbohydrate Antigen (Ca19-9), For Monitoring And Management Of Pancreatic CancerNIG110
- Calibrator, SecondaryJIT94
- Test, Syphilis, TreponemalMTN94
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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