Product Recall  from LTS

This serves as a notification of a recall on behalf of LTS, the manufacturer of the Ionto Patchi STAT® and Ionto Patch 80®. The voluntary recall is due to nonwoven pads in the device not absorbing the saline solution or any other liquid intended to be used with the device.

Note: If you are a distributor, promptly notify any of your customers that may have received affected product. Have the customers return any affected product to you for collection and return to LTS.

Ionto Patch STAT® and Ionto Patch 80®

Nonwoven pads in the device not absorbing the saline solution or any other liquid intended to be used with the device.

Status : Open

Please review the instructions below and submit your response(s) to Performance Health.

Return Instructions

1. Please return all Ionto Patch STAT® (Lot #'s 4283-1, 4283-2, 4283-3, and 4283-4), and 80® (Lot #'s 4303-1, 4303-2, 4303-3) to:
   
   LTS Therapy System, LLC
   IontoPatch
   1685 Marthaler Lane
   West St. Paul, MN 55118
   
   Use: FedEx Account #055409528 Ground Shipment
2. Please notify your customers that have received the IntoPatch STAT® and/or 80® lot #'s listed above and request that they return all inventory remaining of the affected product using the instructions in Step 1.
3. Download and complete Attachment 1 and send to Steve Lento at: steve.leno@ltslohmann.com

Where to find your Lot #