Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cardio Medical Products Recalled by Cardio Medical Products Due to Covidien received customer reports of Arcing/Sparking on the...
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 Cardio Medical Products directly.
Affected Products
Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866 www.cardiomedicalproducts.com (800) 227-3633 (973) 586-9624 FAX Defibrillator
Quantity: 657 units
Why Was This Recalled?
Covidien received customer reports of Arcing/Sparking on the defibrillation electrode leadwire which may affect Cardio Medical Products Inc. defibrillator electrodes Model Number O101.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cardio Medical Products
Cardio Medical Products has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report