Edwards Lifesciences Aquarius Hemodialysis System: Recall

by FDA on February 6, 2010

in MedWatch

Clinically significant fluid imbalance and potential for users to repeatedly override the fluid imbalance alarm.

This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice.

View Full Details Of The Original MedWatch Notice Here.

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