Reported Aug 6, 2025 · Ongoing
IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal…
LTS Therapy Systems, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: LTS Therapy Systems, LLC · 1685 Marthaler Ln · Saint Paul, MN · 55118-3517
Is this the product you have?
- IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.
- Lot codes and dates
- Lot CodeUDI-DI: (01) 10815611020005
- UDI-PI(10) 4283
- Lot numbers
4283-14283-24283-34283-4
- Amount recalled
- 80928 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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