Merit Medical Systems, Inc. Recalls

10 recalls on record in the United States

medical: 10
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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medical Class II
2026-10-07

Merit Medical Systems, Inc. recalls Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, RE

Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, which if used could lead to infection.

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