Relievant Medsystems, Inc.
11 devices · 109 adverse event reports · 3 deaths reported · 5 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.
- Intracept RLV 0055Probe, Radiofrequency Lesion1 recall30 reports
- Intracept RLV 0045Probe, Radiofrequency Lesion1 recall1 death23 reports
- Intracept RLV0065Probe, Radiofrequency Lesion1 recall14 reports
- Intracept RLV 0075Probe, Radiofrequency Lesion1 recall3 reports
- Intracept RLV 0035Probe, Radiofrequency Lesion1 recall0 reports
- Intracept RF Probe RLV 0015Probe, Radiofrequency Lesion2 deaths21 reports
- Intracept FG 0060Probe, Radiofrequency Lesion13 reports
- Intracept FG 0043Probe, Radiofrequency Lesion2 reports
- Intracept FG 0045Probe, Radiofrequency Lesion1 report
- Intracept FG 0046Probe, Radiofrequency Lesion1 report
- Intracept FG 0038Probe, Radiofrequency Lesion1 report