Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IontoPatch 80 Recalled by LTS Therapy Systems, LLC Due to The nonwoven pads in the device do not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact LTS Therapy Systems, LLC directly.
Affected Products
IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.
Quantity: 63936 units
Why Was This Recalled?
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About LTS Therapy Systems, LLC
LTS Therapy Systems, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report