Merit Medical Systems, Inc. recalls

18 recalls.

• Scout MD recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported October 21, 2026 · The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.
• Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported October 7, 2026 · Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the...
• Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 ... recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported June 24, 2026 · Due to unsealed portions of pouches.
• Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire
• Philips Bridge Prep Kit REF: K12-09098C Sterile EO recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire
• Philips Bridge Prep Kit REF: K12-09098B Sterile EO recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported May 6, 2026 · catheter may experience resistance when being advanced over the guidewire
• BioFlo DuraMax Catheter recall (Merit Medical Systems, Inc.)
  Medical deviceClass IReported April 1, 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...
• DuraMax Chronic Hemodialysis Catheter recall (Merit Medical Systems, Inc.)
  Medical deviceClass IReported April 1, 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...
• 16F Dual Valved Splittable Sheath Introducer recall (Merit Medical Systems, Inc.)
  Medical deviceClass IReported April 1, 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...
• ProGuide Chronic Dialysis Catheters recall (Merit Medical Systems, Inc.)
  Medical deviceClass IReported April 1, 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...
• CentrosFLO Hemodialysis Catheters recall (Merit Medical Systems, Inc.)
  Medical deviceClass IReported April 1, 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...
• Allwell Angioplasty Pack REF: IS-30-B1/B recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Merit Medical recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Merit Medical recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Merit Medical recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Merit Medical recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Allwell Inflation Device recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.
• Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers:... recall (Merit Medical Systems, Inc.)
  Medical deviceClass IIReported January 28, 2026 · Inflation device handle may detach from the syringe during procedure.