FDAMay 8, 2023device

Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16

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

The hazard

Sheath introducer assemblies could potentially, due to improper storage conditions, have a luer connection portion of the dilator hub that cracks or dislodges during use, which renders the dilator component unusable, and can require the use of a replacement device.

What to do

FDA enforcement status: Ongoing

Brands named

galt medicalgalt

UPCs

0084126810519500841268105249

Recall history

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

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