Lumiradx UK Ltd.
FDA adverse event reports naming Lumiradx UK Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: LUMIRADX UK LTD..
- Total reports
- 1,783
- Deaths
- 0
- Injuries
- 0
- Malfunctions
- 1,783
Reports per year
1,55421
20322
2323
324
Source: FDA adverse event reports by year received, 2021–2024. 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.
Monitor Lumiradx UK Ltd. automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.