FDAMarch 20, 2020device

LifePAK 500 Automated External Defibrillator, model numbers: 3005400-XXX, U3005400-XXX, 3011790-XXX/, U3011790-XXX - Product Usage: The LIFEPAK 500 AED is a semi-automatic defibrillator that uses a patented Shock Advisory System. This software algorithm analyzes the patient s electrocardiographic...

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

The hazard

Automated External Defibrillators may not detect a patient connection due to mechanical wear-through of the contact plating on the therapy connector. The wear-through could result in the device not recognizing a patient is connected which could result in a delay in treatment

What to do

FDA enforcement status: Terminated

Brands named

physio controlphysiophysio control

Recall history

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

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