FDAMay 14, 2024device

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

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

The hazard

Devices were labelled with the incorrect guidewire labelling.

What to do

FDA enforcement status: Completed

Brands named

applied medical technologyappliedapplied medical

UPCs

00842071131876

Recall history

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

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