Merit Medical Systems, Inc. Recalls

9 recalls on record in the United States

medical: 9
medical Class I
2026-04-01

Merit Medical Systems, Inc. recalls CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K

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.

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medical Class I
2026-04-01

Merit Medical Systems, Inc. recalls ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21

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.

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medical Class I
2026-04-01

Merit Medical Systems, Inc. recalls 16F Dual Valved Splittable Sheath Introducer (bulk, non-ster

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.

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medical Class I
2026-04-01

Merit Medical Systems, Inc. recalls BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021

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.

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medical Class I
2026-04-01

Merit Medical Systems, Inc. recalls DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A,

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.

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medical Class II
2026-05-06

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONL

catheter may experience resistance when being advanced over the guidewire

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medical Class II
2026-05-06

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONL

catheter may experience resistance when being advanced over the guidewire

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medical Class II
2026-05-06

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONL

catheter may experience resistance when being advanced over the guidewire

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medical Class II
2026-06-24

Merit Medical Systems, Inc. recalls Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-D

Due to unsealed portions of pouches.

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