Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MINI INFANT < 3KG Recalled by ConMed Corporation Due to Wire sets of certain devices were assembled with...
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 ConMed Corporation directly.
Affected Products
MINI INFANT < 3KG, RADIOTRANSLUCENT ELECTRODE, Universal/Anderson Connector, REF/Catalog Number 2602 Indicated for use in external pacing, defibrillation and monitoring applications as a non-sterile, disposable device for single pediatric use, only. The PadPro 2602 electrodes provide the conductive interface between the defibrillator and/or the external transcutaneous (non-invasive) cardiac pacemaker and the pediatric patients skin. The electrode is intended for use on pediatric infants whose weight is less than 10 kg. (22 lbs.).
Quantity: 18,720 units in total
Why Was This Recalled?
Wire sets of certain devices were assembled with adhesive on the contact wires, which may impede conductivity and could cause failure
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ConMed Corporation
ConMed Corporation has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report