PFAClass 2
Non-Invasive Central Venous Manometer
FDA adverse event reports and recall history for non-invasive central venous manometer (product code PFA), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 117
- Deaths
- 0
- Injuries
- 52
- Malfunctions
- 65
Reports per year
2824
3825
5126
Source: FDA adverse event reports by year received, 2024–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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