BfArM - Federal Institute for Drugs and Medical Devices

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Product group Medical electronics / Electromedical devices
Reference 00529/05

Medtronic has initiated a recall on a specific group of monophasic LIFEPAK 500 automated external defibrillator manufactured between March and May 1997.The AED may continue to display a "connect electrodes" message and may not analyze the patient's heart rhythm even when the electrodes are properly connected.

Medtronic recalls LIFEPAK 500 , Download_VeroeffentlichtAm_EN PDF, 30KB,