FDAMay 22, 2025device

IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.

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

The hazard

The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.

What to do

FDA enforcement status: Ongoing

Brands named

lts therapy systemsltslts therapy

UPCs

10815611020012

Recall history

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

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