Abbott Diabetes Care Ltd
FDA adverse event reports naming Abbott Diabetes Care Ltd as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ABBOTT DIABETES CARE LTD.
- Total reports
- 105,960
- Deaths
- 37
- Injuries
- 11,506
- Malfunctions
- 94,417
Reports per year
114
116
117
1818
820
2321
1,60622
8,02223
11,51224
12,08225
72,68626
Source: FDA adverse event reports by year received, 2014–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Integrated Continuous Glucose Monitoring System, Factory CalibratedQBJ84,512
- Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery SystemsQLG21,341
- Sensor, Glucose, Invasive, Non-Adjunctive, Factory-Calibrated, User-InitiatedPZE49
- Patient Monitor With Independent Remote Display And OperationQLJ27
- System, Test, Blood Glucose, Over The CounterNBW12
- Continuous Glucose Monitor Secondary DisplayPJT7
- Sensor, Glucose, InvasiveMDS4
- Continuous Glucose Monitor Retrospective Data Analysis SoftwarePHV2
- Assay, Oral Direct Thrombin InhibitorQBG2
- Piston Syringe LeverQBL2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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