PKUClass 2
Insulin Pump Secondary Display
FDA adverse event reports and recall history for insulin pump secondary display (product code PKU), from the public MAUDE/AEMS corpus and the live FDA recall database.
- Total reports
- 37,977
- Deaths
- 0
- Injuries
- 43
- Malfunctions
- 37,934
Reports per year
6,03622
10,08323
9,64824
12,02325
18726
Source: FDA adverse event reports by year received, 2022–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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