Merit Medical Systems, Inc
12701 Kingston Avenue, Chester, VA, US
Registered product codes
14 product codes
Recent MDR events
6,716 on file
- ClariVein® OCJul 30, 2026Malfunction1721504-2026-00401
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00040
- AERO®.StentJul 30, 2026Malfunction3010665433-2026-00034
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00035
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00036
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00037
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00039
- AEROmini®.StentJul 30, 2026Malfunction3010665433-2026-00038
- BioSentry®Jul 29, 2026Injury3010665433-2026-00033
- BioSentry®Jul 29, 2026Injury3010665433-2026-00032
Recalls
299 on file
- Open, ClassifiedJun 18, 2026
Due to unsealed portions of pouches.
View FDA record ↗ - Open, ClassifiedApr 29, 2026
catheter may experience resistance when being advanced over the guidewire
View FDA record ↗ - Open, ClassifiedApr 29, 2026
catheter may experience resistance when being advanced over the guidewire
View FDA record ↗ - Open, ClassifiedApr 29, 2026
catheter may experience resistance when being advanced over the guidewire
View FDA record ↗ - Open, ClassifiedMar 26, 2026
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
View FDA record ↗ - Open, ClassifiedMar 26, 2026
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
View FDA record ↗ - Open, ClassifiedMar 26, 2026
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
View FDA record ↗ - Open, ClassifiedMar 26, 2026
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
View FDA record ↗ - Open, ClassifiedMar 26, 2026
16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies, procedure delay, embolization/thrombosis, impaired catheter function, loss of vessel for future vascular access.
View FDA record ↗ - Open, ClassifiedJan 16, 2026
Inflation device handle may detach from the syringe during procedure.
View FDA record ↗
Compliance history
Matched by FEI 3002975287.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.