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LTS Therapy Systems, LLC recalls IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal pa
Recalled August 6, 2025 · FDA recall Z-2196-2025 · LTS Therapy Systems
Hazard
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device. · FDA Class II
Units
80928 units
Sold at
US Nationwide distribution in the states of Indiana, Tennessee, New York, Minnesota, New Jersey, Ohio, Kentucky, Illinois, and South Dakota.
Description
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
Product
IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
Manufacturer(s)
LTS Therapy Systems, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →