LTS Therapy Systems recalls IontoPatch 80 patches (model D-0077-080) due to nonwoven pads failing to absorb saline solution, risking ineffective treatment. Affected units sold with lot numbers 4303-1, 4303-2, 4303-3.
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
LTS Therapy Systems recalls IontoPatch 80 patches because the nonwoven pads don't absorb saline solution properly. This could lead to ineffective treatment as the medication isn't delivered correctly. Users should check their product's lot numbers to see if they're affected.
The nonwoven pads in the IontoPatch 80 fail to absorb saline solution, meaning medication won't be delivered properly through the skin. This could result in ineffective treatment for conditions requiring consistent medication delivery.
Users of the IontoPatch 80 patches for transdermal therapy are affected. People with specific medical conditions requiring consistent medication delivery are at higher risk.
Check for the model number D-0077-080 on the patch. Affected units have lot numbers 4303-1, 4303-2, or 4303-3.
Look for lot numbers 4303-1, 4303-2, or 4303-3 on the patch packaging.
The nonwoven pads in the IontoPatch 80 do not absorb saline solution properly, which could lead to ineffective medication delivery.
Check the lot number on your patch. If it's 4303-1, 4303-2, or 4303-3, contact LTS Therapy Systems for instructions.
The recall record does not mention a fix or remedy for this issue.
We’ve drafted a message you can send LTS Therapy Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2197-2025 — LTS Therapy Systems LTS Therapy Systems Hello, I own a LTS Therapy Systems that is covered by recall Z-2197-2025 from LTS Therapy Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
