FDAJune 12, 2019device

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 ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a potential for the device to fail to deliver energy to the patient.

What to do

FDA enforcement status: Ongoing

Brands named

zoll medicalzoll

UPCs

0084794601612800847946016142008479460151380084794601613500847946016166

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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