CareFusion Alaris PC Unit, Model 8015: Class I Recall – Error Code

by FDA on August 1, 2012

in MedWatch

Potential error code may cause a delay in patient therapy or result in serious injury and/or death to the patient.

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.

Leave a Comment

Previous post:

Next post: