LTS Therapy Systems IontoPatch 80, On-the-Go Patch Therapy recall — FDA Z-2197-2025
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
Overview of recall records associated with LTS Therapy Systems, LLC, including dates, categories and classifications where available.
Classification mix: Class II: 2.
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.
This page summarizes recall records in which the official source identifies LTS Therapy Systems, LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.