Lifescan Europe, A Division OF Cilag Gmbh Intl
FDA adverse event reports naming Lifescan Europe, A Division OF Cilag Gmbh Intl as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL.
- Total reports
- 223,383
- Deaths
- 4
- Injuries
- 9,366
- Malfunctions
- 213,314
Reports per year
99811
8,37712
32,98013
35,38214
55,25415
64,69716
22,83417
2,80218
5919
Source: FDA adverse event reports by year received, 2011–2019. 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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