LHIClass 2
Set, I.V. Fluid Transfer
FDA adverse event reports and recall history for set, i.v. fluid transfer (product code LHI), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 14,331
- Deaths
- 20
- Injuries
- 349
- Malfunctions
- 13,798
Reports per year
52912
15413
15514
12815
21916
53617
1,49918
1,63419
1,17120
93321
1,83422
1,04723
1,27024
1,35625
93526
Source: FDA adverse event reports by year received, 2012–2026. 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.
Monitor set, i.v. fluid transfer 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.