Merit Medical Systems, Inc.

Frequent Recalls

9

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-04-01 to 2026-06-24

Date	Source	Product	Brand	Severity	Units
2026-06-24	FDA Device	FDA Recall: Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669	Merit Medical Systems, Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY	Merit Medical Systems, Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY	Merit Medical Systems, Inc.	Class II	N/A
2026-05-06	FDA Device	FDA Recall: Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY	Merit Medical Systems, Inc.	Class II	N/A
2026-04-01	FDA Device	FDA Recall: ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-N	Merit Medical Systems, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A,	Merit Medical Systems, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: 16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B	Merit Medical Systems, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H	Merit Medical Systems, Inc.	Class I	N/A
2026-04-01	FDA Device	FDA Recall: DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A, H787103028025/A, H787103028031/A, H7871	Merit Medical Systems, Inc.	Class I	N/A

Merit Medical Systems, Inc. Recalls | WatchRecall