Iradimed Corp.
5 devices · 24 adverse event reports · 2 deaths reported · 1 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Iradimed 1057Pump, Infusion1 recall7 reports
- Iradimed 3860+Pump, Infusion1 death13 reports
- Iradimed 1056Pump, Infusion2 reports
- Iradimed 3880-3Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)1 death1 report
- Iradimed 3883-2Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)1 report