FDAFebruary 13, 2026device

ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

merit medical systemsmeritmerit medical

UPCs

0088445069787000884450697900008844506978940088445069792400884450697917008844506979480088445069796200884450697979

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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