Integra Lifesciences Switzerland SAR
FDA adverse event reports naming Integra Lifesciences Switzerland SAR as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: INTEGRA LIFESCIENCES SWITZERLAND SAR.
- Total reports
- 2,323
- Deaths
- 22
- Injuries
- 1,755
- Malfunctions
- 546
Reports per year
16319
55120
49421
53122
34023
12624
8025
3826
Source: FDA adverse event reports by year received, 2019–2026. 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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