FDADecember 1, 2016device

PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE Hydrophilic Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries, including but not limited to the radial artery, while maintaining hemosta...

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

The hazard

Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath Introducer because the dilator tips were manufactured with an undersized inner diameter and therefore will not allow passage of an 0.021 (0.53 mm) guide wire.

What to do

FDA enforcement status: Terminated

Brands named

merit medical systemsmeritmerit medical

Recall history

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

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