Reported Apr 1, 2026 · Ongoing
ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C,…
Merit Medical Systems, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Merit Medical Systems, Inc. · 1600 W Merit Pkwy · South Jordan, UT · 84095-2416
Is this the product you have?
- ProGuide Chronic Dialysis Catheters
- REF
DC01455550/CDC21452419/CDC21452419-NE5/CDC21452823-NE5/CDC21454035/CDC21455550/C
- Lot codes and dates
4 of 4 products
Products covered by this recall # Barcodes Product as published 1 00884450697870REF:UDI-DI/Lot(Expiration): DC01455550/C:00884450697870/H2600169 2 008844506979000088445069789400884450697924DC21452419/C:00884450697900/H2659228: DC21452419-NE5/C:00884450697894/H3249278): DC21452823/C:00884450697924/H2600164, H2628890 3 0088445069791700884450697948DC21452823-NE5/C:00884450697917/H2990807: DC21453227/C:00884450697948/H2630602 4 0088445069796200884450697979DC21454035/C:00884450697962/H2628887: DC21455550/C:00884450697979/H2630553, H2659229 - Amount recalled
- 131
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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