Class II
Medical Device Recall: IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The 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
63936 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2197-2025
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.