Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ZOLL AED PRO Automated External Defibrillator Product Usage: The AED Recalled by ZOLL Medical Corporation Due to There is a potential for the device to...
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 ZOLL Medical Corporation directly.
Affected Products
ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate victims of ventricular fibrillation or pulseless ventricular tachycardia, for ECG monitoring, and for CPR monitoring of patients. The CPR monitoring function provides a metronome designed to encourage rescuers to perform chest compressions at the AHA/ERC recommended rate of 100 compressions per minute. Voice and visual prompts encourage a compression depth of at least 2 inches (5 cm) for adult patients. The AED PRO system is indicated for use on victims of cardiac arrest with apparent lack of circulation as indicated by: Unconsciousness Absence of breathing, and Absence of pulse and other signs of circulation. The device is also indicated for use when ECG monitoring is indicated to evaluate the patient s heart rate or ECG morphology. The AED PRO system is indicated for adult and pediatric patients.
Quantity: 1,969
Why Was This Recalled?
There is a potential for the device to fail to deliver energy to the patient.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ZOLL Medical Corporation
ZOLL Medical Corporation has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report