Reshape Lifesciences
FDA adverse event reports naming Reshape Lifesciences as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: RESHAPE LIFESCIENCES.
- Total reports
- 1,142
- Deaths
- 26
- Injuries
- 815
- Malfunctions
- 301
Reports per year
317
1818
7119
3320
6421
24622
62223
7824
725
Source: FDA adverse event reports by year received, 2017–2025. 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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