Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used Recalled by ZOLL Medical Corporation Due to Shipped with incorrect software
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 X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by qualified medical personnel for the purpose of converting ventricular fibrillation to sinus rhythm or other cardiac rhythms capable of producing hemodynamically significant heart beats. In addition, the product may be used in synchronized mode to terminate certain atrial and ventricular tachycardias and other arrhythmias resistant to drug therapy. The X Series may be used for cardiac pacing in conscious or unconscious patients for up to a few hours duration as an alternative to endocardial stimulation. The X Series may be used for the monitoring a patients electrocardiogram (ECG).
Quantity: 11 units
Why Was This Recalled?
Shipped with incorrect software
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