Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien LLC dba Uni-Patch Due to Covidien is conducting a voluntary recall regarding specific...
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 Covidien LLC dba Uni-Patch directly.
Affected Products
Empi STIMC RE Self Adhesive electrodes. For use on TENS, NMES, FES. a DJO brand A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., electroencephalogram) or to apply electrical stimulation.
Quantity: 28,138 pouches
Why Was This Recalled?
Covidien is conducting a voluntary recall regarding specific lots of TENS electrodes because it was determined that during the manufacturing process the surface of the wires in these lots may have been exposed to an employee who had a minor cut.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LLC dba Uni-Patch
Covidien LLC dba Uni-Patch has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report