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
Senior Director Medical Affairs
Edwards Lifesciences
Irvine, CA
Senior Scientist - Cell Engineering Group
Pfizer
San Francisco, CA
Medical Director - Physician
Willamette Valley Community Health
Salem, OR
Area Reimbursement Manager (CT, MA, MD, ME, NH, NJ, NY, PA, VT)
SI-BONE, INC
Multiple Locations, SL_Multiple Locations
Medical Director - Physician
Willamette Valley Community Health
Salem, OR