Animas Corp.
FDA adverse event reports naming Animas Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ANIMAS CORP..
- Total reports
- 6,836
- Deaths
- 66
- Injuries
- 2,039
- Malfunctions
- 4,673
Reports per year
2002
14903
6404
21705
43406
52707
72908
42809
2,33010
1,91711
213
414
415
116
118
Source: FDA adverse event reports by year received, 2002–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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