Class II

Medical Device Recall: IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

LTS Therapy Systems, LLC · May 22, 2025

Reason for Recall

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

Distribution

US Nationwide distribution in the states of Indiana, Tennessee, New York, Minnesota, New Jersey, Ohio, Kentucky, Illinois, and South Dakota.

States Affected

NATIONWIDE

Quantity Affected

80928 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2196-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

LTS Therapy Systems, LLC Medical Device Recall: IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch. | SafeCheck