FDAAugust 1, 2022device

6" (15 cm) Appx 0.85 ml, Smallbore Trifuse Ext Set w/3 MicroClave Clear, 2 Check Valve, 3 Clamps, Rotating Luer;

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

The hazard

Due to a manufacturing defect which results in a visible gap between the connector's top and bottom housing.

What to do

FDA enforcement status: Ongoing

Brands named

icu medicalicu

Recall history

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

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