Recall
FDAHealthMay 22, 2025

LTS Therapy Systems, LLC — IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 22, 2025

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

What's affected?

Product
IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
Lot code
UDI-DI:

Additional details

Lot Code: UDI-DI: (01) 10815611020005 UDI-PI: (10) 4283 Lot numbers: 4283-1, 4283-2, 4283-3, 4283-4

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 80928 units.

View original FDA notice →

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