I-flow Corp.
FDA adverse event reports naming I-flow Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: I-FLOW CORP..
- Total reports
- 1,472
- Deaths
- 13
- Injuries
- 368
- Malfunctions
- 233
Reports per year
1000
501
902
2503
4404
9005
6006
6207
17408
22209
26710
32111
8612
2913
2814
Source: FDA adverse event reports by year received, 2000–2014. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, Infusion, ElastomericMEB1,299
- Catheter, Conduction, AnestheticBSO94
- Pump, InfusionFRN44
- Set, Administration, IntravascularFPA13
- Introducer, CatheterDYB11
- Pump, Infusion, PcaMEA6
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ2
- Transducer, Ultrasonic, DiagnosticITX1
- Stimulator, Nerve, Peripheral, ElectricKOI1
- Pump, Infusion, Implanted, ProgrammableLKK1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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