FDAMarch 27, 2025device

GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vasculature.

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

The hazard

Due to a potential open seal in the sterile barrier packaging.

What to do

FDA enforcement status: Ongoing

Brands named

galt medicalgalt

UPCs

0084126810132

Recall history

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

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