Pulmonx Corporation
FDA adverse event reports naming Pulmonx Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PULMONX CORPORATION.
- Total reports
- 1,194
- Deaths
- 166
- Injuries
- 935
- Malfunctions
- 93
Reports per year
1318
21219
7520
10321
32122
22623
12324
7625
4526
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused twice in 2026 during FDA reporting-system changes 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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