FDA recalls 2 ventilator models

12/27/2012 | MedPage Today (free registration)

The FDA has recalled two ventilator-related devices. The Ventlab manual resuscitator was found to have a potentially leaking valve that could result in little or no airflow to the patient. The Bunnell Life Pulse High-Frequency Ventilator Patient Circuit, used for critically ill infants, has heater wire insulation that can melt, causing sparking and smoke.

View Full Article in:

MedPage Today (free registration)

Published in Briefs:

SmartBrief Job Listings for Health Care

Job Title Company Location
Counsel – Regulatory Affairs
RAI Services Company
Winston Salem, NC
Director of Program Development
AdvaMed
Washington DC, DC
Director of System QA
LifeWatch Services, Inc.
Rosemont, IL
Director of Business Development and Membership
AdvaMed
Washington DC, DC
Director, Corporate Counsel
Regeneron
Tarrytown, NY