Lifescan Europe Gmbh
FDA adverse event reports naming Lifescan Europe Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LIFESCAN EUROPE GMBH.
- Total reports
- 5,424
- Deaths
- 0
- Injuries
- 2,224
- Malfunctions
- 3,188
Reports per year
2613
1015
416
42018
3,56219
49920
40221
15222
16023
12324
4425
2226
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Test, Blood Glucose, Over The CounterNBW5,319
- Glucose Oxidase, GlucoseCGA50
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK37
- Pump, Infusion, InsulinLZG8
- Glucose Dehydrogenase, GlucoseLFR7
- Single (Specified) Analyte Controls (Assayed And Unassayed)JJX2
- Sensor, Glucose, InvasiveMDS1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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